Disease: Mean Corpuscular Volume (result)
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34523089
RNF43 ; TSPOAP1-AS1
17 58358748 missense variant C/T snv 0.11 0.11 2
rs34544423 1 198578103 regulatory region variant C/G snv 6.4E-02 2
rs35091702
RBPMS
8 30421955 intron variant GAAAAAA/- delins 0.78 2
rs35229050
E2F2
1 23514124 intron variant AA/-;A;AAA delins 0.53 2
rs35340377
TRIM58
1 247874908 intron variant G/A snv 0.23 2
rs35676364
ILKAP
2 238184733 intron variant TTTTT/-;TTTT;TTTTTT;TTTTTTT;TTTTTTTT delins 2
rs35998524 5 154655677 intergenic variant C/T snv 7.4E-02 2
rs3962382 1 67700010 downstream gene variant A/C;G snv 2
rs41444548
TBX21
17 47733988 intron variant C/G snv 4.6E-02 4.4E-02 2
rs4771651
LOC105370360
13 109804341 intron variant G/A snv 0.36 2
rs4822191 22 42745014 intergenic variant G/A snv 0.44 2
rs4848370
ACOXL ; MIR4435-2HG
2 111054088 intron variant C/T snv 0.25 2
rs4900538
LOC105370680
14 102527728 intergenic variant T/A;C;G snv 2
rs5030755
RPA1
17 1879658 missense variant A/G snv 7.6E-02 7.4E-02 2
rs549220260
CHAF1A
19 4426168 intron variant TTTTTTTT/-;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT delins 2
rs550548705 16 67889570 upstream gene variant AAAAAAAAAAAAA/-;AAA;AAAAAA;AAAAAAAAA;AAAAAAAAAAAA;AAAAAAAAAAAAAA;AAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAAAAAAAAAAA delins 4.4E-02 2
rs572017140
KAT7
17 49797971 intron variant G/A snv 4.2E-05 2
rs5749446
FBXO7
22 32484598 intron variant T/A;C snv 2
rs59883166
LOC643339
12 93364543 intron variant T/-;TT;TTT delins 2
rs6060987 20 31839274 downstream gene variant T/A snv 0.29 2
rs60718933
SOX6
11 16017007 intron variant T/A;C snv 2
rs607203 6 139520516 intron variant T/C snv 0.91 2
rs6073966
PCIF1
20 45941553 intron variant C/T snv 0.11 2
rs61358232 13 109749719 downstream gene variant A/T snv 0.27 2
rs6147862
LRIG1
3 66402550 intron variant GCATGGTGGGAAGGACCCAAGGT/-;GCATGGTGGGAAGGACCCAAGGTGCATGGTGGGAAGGACCCAAGGT delins 0.60 2