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rs121912755

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912755(A;A)
Make rs121912755(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position44253150
GeneSLC4A1
is asnp
is mentioned by
dbSNPrs121912755
ebirs121912755
HLIrs121912755
Exacrs121912755
Varsomers121912755
Maprs121912755
PheGenIrs121912755
hapmaprs121912755
1000 genomesrs121912755
hgdprs121912755
ensemblrs121912755
gopubmedrs121912755
geneviewrs121912755
scholarrs121912755
googlers121912755
pharmgkbrs121912755
gwascentralrs121912755
openSNPrs121912755
23andMers121912755
23andMe allrs121912755
SNP Nexus

SNPshotrs121912755
SNPdbers121912755
MSV3drs121912755
GWAS Ctlgrs121912755
Max Magnitude0
OMIM109270
Desc
Variant0028
Relatedalso
ClinVar
Risk rs121912755(A;A)
Alt rs121912755(A;A)
Reference rs121912755(G;G)
Significance Pathogenic
Disease Spherocytosis type 4
Variation info
Gene SLC4A1
CLNDBN Spherocytosis type 4
Reversed 1
HGVS NC_000017.10:g.42330518C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019358.30,