rs4141463
|
|
|
0.820 |
GeneticVariation |
BEFREE |
Therefore, this family-based association study was performed in 640 Chinese Han autism trios to investigate the association between autism and 7 SNPs with genome-wide significance in previous GWAS (rs4307059 near MSNP1AS, rs4141463 in MACROD2, rs2535629 in ITIH3, rs11191454 in AS3MT, rs1625579 in MIR137HG, rs11191580 in NT5C2, and rs1409313 in CUEDC2).
|
30610940 |
2019 |
rs4141463
|
|
|
0.820 |
GeneticVariation |
BEFREE |
Therefore, this study does not provide support for the reported association between rs4141463 and autism.
|
21656903 |
2011 |
rs4141463
|
|
|
0.820 |
GeneticVariation |
GWASCAT |
A genome-wide scan for common alleles affecting risk for autism.
|
20663923 |
2010 |
rs4141463
|
|
|
0.820 |
GeneticVariation |
GWASDB |
A genome-wide scan for common alleles affecting risk for autism.
|
20663923 |
2010 |
rs4307059
|
|
|
0.810 |
GeneticVariation |
BEFREE |
The results showed a nominal association between the T allele of rs4307059 and autism under both additive model (T>C, Z = 2.250, P = .024) and recessive model (T>C, Z = 2.109, P = .035).
|
30610940 |
2019 |
rs1877455
|
|
|
0.810 |
GeneticVariation |
BEFREE |
Meta-analysis identified three single-nucleotide polymorphisms, rs936938 (P=4.49 × 10(-8)), non-synonymous rs6537835 (P=3.26 × 10(-8)) and rs1877455 (P=8.70 × 10(-8)), and related haplotypes, AMPD1-NRAS-CSDE1, TRIM33 and TRIM33-BCAS2, associated with autism; all were mapped to a previously reported linkage region (1p13.2) with autism.
|
24189344 |
2014 |
rs1877455
|
|
T |
0.810 |
GeneticVariation |
GWASDB |
Meta-analysis identified three single-nucleotide polymorphisms, rs936938 (P=4.49 × 10(-8)), non-synonymous rs6537835 (P=3.26 × 10(-8)) and rs1877455 (P=8.70 × 10(-8)), and related haplotypes, AMPD1-NRAS-CSDE1, TRIM33 and TRIM33-BCAS2, associated with autism; all were mapped to a previously reported linkage region (1p13.2) with autism.
|
24189344 |
2014 |
rs1877455
|
|
A |
0.810 |
GeneticVariation |
GWASDB |
Meta-analysis identified three single-nucleotide polymorphisms, rs936938 (P=4.49 × 10(-8)), non-synonymous rs6537835 (P=3.26 × 10(-8)) and rs1877455 (P=8.70 × 10(-8)), and related haplotypes, AMPD1-NRAS-CSDE1, TRIM33 and TRIM33-BCAS2, associated with autism; all were mapped to a previously reported linkage region (1p13.2) with autism.
|
24189344 |
2014 |
rs1877455
|
|
T |
0.810 |
GeneticVariation |
GWASCAT |
Meta-analysis identified three single-nucleotide polymorphisms, rs936938 (P=4.49 × 10(-8)), non-synonymous rs6537835 (P=3.26 × 10(-8)) and rs1877455 (P=8.70 × 10(-8)), and related haplotypes, AMPD1-NRAS-CSDE1, TRIM33 and TRIM33-BCAS2, associated with autism; all were mapped to a previously reported linkage region (1p13.2) with autism.
|
24189344 |
2014 |
rs4307059
|
|
T |
0.810 |
GeneticVariation |
GWASDB |
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
|
19404256 |
2009 |
rs4307059
|
|
T |
0.810 |
GeneticVariation |
GWASCAT |
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
|
19404256 |
2009 |
rs10489525
|
|
G |
0.800 |
GeneticVariation |
GWASCAT |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |
rs10489525
|
|
G |
0.800 |
GeneticVariation |
GWASDB |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |
rs11102800
|
|
C |
0.800 |
GeneticVariation |
GWASDB |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |
rs11102800
|
|
C |
0.800 |
GeneticVariation |
GWASCAT |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |
rs11102807
|
|
A |
0.800 |
GeneticVariation |
GWASDB |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |
rs11102807
|
|
A |
0.800 |
GeneticVariation |
GWASCAT |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |
rs11582563
|
|
G |
0.800 |
GeneticVariation |
GWASCAT |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |
rs11582563
|
|
G |
0.800 |
GeneticVariation |
GWASDB |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |
rs11585926
|
|
T |
0.800 |
GeneticVariation |
GWASDB |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |
rs11585926
|
|
T |
0.800 |
GeneticVariation |
GWASCAT |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |
rs11587400
|
|
C |
0.800 |
GeneticVariation |
GWASCAT |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |
rs11587400
|
|
C |
0.800 |
GeneticVariation |
GWASDB |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |
rs11589568
|
|
T |
0.800 |
GeneticVariation |
GWASCAT |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |
rs11589568
|
|
T |
0.800 |
GeneticVariation |
GWASDB |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |