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rs75731670

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs75731670(C;T)
Make rs75731670(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position44254581
GeneSLC4A1
is asnp
is mentioned by
dbSNPrs75731670
ebirs75731670
HLIrs75731670
Exacrs75731670
Varsomers75731670
Maprs75731670
PheGenIrs75731670
hapmaprs75731670
1000 genomesrs75731670
hgdprs75731670
ensemblrs75731670
gopubmedrs75731670
geneviewrs75731670
scholarrs75731670
googlers75731670
pharmgkbrs75731670
gwascentralrs75731670
openSNPrs75731670
23andMers75731670
23andMe allrs75731670
SNP Nexus

SNPshotrs75731670
SNPdbers75731670
MSV3drs75731670
GWAS Ctlgrs75731670
Merged fromRs121912740
GMAF0.0
Max Magnitude0
ClinVar
Risk rs75731670(T;T)
Alt rs75731670(T;T)
Reference rs75731670(C;C)
Significance Other
Disease BLOOD GROUP--WRIGHT ANTIGEN
Variation info
Gene SLC4A1
CLNDBN BLOOD GROUP--WRIGHT ANTIGEN
Reversed 0
HGVS NC_000017.10:g.42331949C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019336.28,