Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1057519946
rs1057519946
0.732 0.280 19 52212729 missense variant C/G;T snv
CUI: C0007112
Disease: Adenocarcinoma of prostate
Adenocarcinoma of prostate
0.700 1.000 1 2016 2016
dbSNP: rs1057519946
rs1057519946
0.732 0.280 19 52212729 missense variant C/G;T snv
CUI: C0280630
Disease: Uterine Carcinosarcoma
Uterine Carcinosarcoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519946
rs1057519946
0.732 0.280 19 52212729 missense variant C/G;T snv
CUI: C0279663
Disease: Serous cystadenocarcinoma ovary
Serous cystadenocarcinoma ovary
0.700 1.000 1 2016 2016
dbSNP: rs1057519946
rs1057519946
0.732 0.280 19 52212729 missense variant C/G;T snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs1057519946
rs1057519946
0.732 0.280 19 52212729 missense variant C/G;T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 1.000 1 2016 2016
dbSNP: rs1057519946
rs1057519946
0.732 0.280 19 52212729 missense variant C/G;T snv
Squamous cell carcinoma of the head and neck
0.700 1.000 1 2016 2016
dbSNP: rs1057519946
rs1057519946
0.732 0.280 19 52212729 missense variant C/G;T snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs1057519946
rs1057519946
0.732 0.280 19 52212729 missense variant C/G;T snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519946
rs1057519946
0.732 0.280 19 52212729 missense variant C/G;T snv
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs1057519946
rs1057519946
0.732 0.280 19 52212729 missense variant C/G;T snv
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs1057519946
rs1057519946
0.732 0.280 19 52212729 missense variant C/G;T snv
MENTAL RETARDATION, AUTOSOMAL DOMINANT 36
0.700 0
dbSNP: rs1057519946
rs1057519946
0.732 0.280 19 52212729 missense variant C/G;T snv
CUI: C0026010
Disease: Microphthalmos
Microphthalmos
0.700 0
dbSNP: rs1057519946
rs1057519946
0.732 0.280 19 52212729 missense variant C/G;T snv
CUI: C1856888
Disease: Clinodactyly of the thumb
Clinodactyly of the thumb
0.700 0
dbSNP: rs1057519946
rs1057519946
0.732 0.280 19 52212729 missense variant C/G;T snv
CUI: C0855329
Disease: Electrocardiogram change
Electrocardiogram change
0.700 0
dbSNP: rs1057519946
rs1057519946
0.732 0.280 19 52212729 missense variant C/G;T snv
CUI: C2243051
Disease: Large head (disorder)
Large head (disorder)
0.700 0
dbSNP: rs1057519946
rs1057519946
0.732 0.280 19 52212729 missense variant C/G;T snv
CUI: C2936786
Disease: Aqueductal Stenosis
Aqueductal Stenosis
0.700 0
dbSNP: rs1057519946
rs1057519946
0.732 0.280 19 52212729 missense variant C/G;T snv
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus
0.700 0
dbSNP: rs1057519947
rs1057519947
0.790 0.160 19 52212730 missense variant G/A snv
CUI: C0280630
Disease: Uterine Carcinosarcoma
Uterine Carcinosarcoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519947
rs1057519947
0.790 0.160 19 52212730 missense variant G/A snv
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs1057519947
rs1057519947
0.790 0.160 19 52212730 missense variant G/A snv
CUI: C0279663
Disease: Serous cystadenocarcinoma ovary
Serous cystadenocarcinoma ovary
0.700 1.000 1 2016 2016
dbSNP: rs1057519947
rs1057519947
0.790 0.160 19 52212730 missense variant G/A snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.700 1.000 1 2016 2016
dbSNP: rs1057519947
rs1057519947
0.790 0.160 19 52212730 missense variant G/A snv
CUI: C0007112
Disease: Adenocarcinoma of prostate
Adenocarcinoma of prostate
0.700 1.000 1 2016 2016
dbSNP: rs1057519947
rs1057519947
0.790 0.160 19 52212730 missense variant G/A snv
Squamous cell carcinoma of the head and neck
0.700 1.000 1 2016 2016
dbSNP: rs1057519947
rs1057519947
0.790 0.160 19 52212730 missense variant G/A snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519947
rs1057519947
0.790 0.160 19 52212730 missense variant G/A snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2016 2016