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rs121912743

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912743(A;A)
Make rs121912743(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position44255804
GeneSLC4A1
is asnp
is mentioned by
dbSNPrs121912743
ebirs121912743
HLIrs121912743
Exacrs121912743
Varsomers121912743
Maprs121912743
PheGenIrs121912743
hapmaprs121912743
1000 genomesrs121912743
hgdprs121912743
ensemblrs121912743
gopubmedrs121912743
geneviewrs121912743
scholarrs121912743
googlers121912743
pharmgkbrs121912743
gwascentralrs121912743
openSNPrs121912743
23andMers121912743
23andMe allrs121912743
SNP Nexus

SNPshotrs121912743
SNPdbers121912743
MSV3drs121912743
GWAS Ctlgrs121912743
Max Magnitude0
OMIM109270
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121912743(A;A)
Alt rs121912743(A;A)
Reference rs121912743(G;G)
Significance Other
Disease BLOOD GROUP--WALDNER TYPE
Variation info
Gene SLC4A1
CLNDBN BLOOD GROUP--WALDNER TYPE
Reversed 1
HGVS NC_000017.10:g.42333172C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019334.26,