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rs121912756

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912756(A;A)
Make rs121912756(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position44257538
GeneSLC4A1
is asnp
is mentioned by
dbSNPrs121912756
ebirs121912756
HLIrs121912756
Exacrs121912756
Varsomers121912756
Maprs121912756
PheGenIrs121912756
hapmaprs121912756
1000 genomesrs121912756
hgdprs121912756
ensemblrs121912756
gopubmedrs121912756
geneviewrs121912756
scholarrs121912756
googlers121912756
pharmgkbrs121912756
gwascentralrs121912756
openSNPrs121912756
23andMers121912756
23andMe allrs121912756
SNP Nexus

SNPshotrs121912756
SNPdbers121912756
MSV3drs121912756
GWAS Ctlgrs121912756
Max Magnitude0
OMIM109270
Desc
Variant0029
Relatedalso
ClinVar
Risk rs121912756(A;A)
Alt rs121912756(A;A)
Reference rs121912756(G;G)
Significance Other
Disease BLOOD GROUP--FROESE
Variation info
Gene SLC4A1
CLNDBN BLOOD GROUP--FROESE
Reversed 1
HGVS NC_000017.10:g.42334906C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019359.29,