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rs863225468

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225468(C;C)
Make rs863225468(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position49619326
GeneRHAG
is asnp
is mentioned by
dbSNPrs863225468
ebirs863225468
HLIrs863225468
Exacrs863225468
Varsomers863225468
Maprs863225468
PheGenIrs863225468
hapmaprs863225468
1000 genomesrs863225468
hgdprs863225468
ensemblrs863225468
gopubmedrs863225468
geneviewrs863225468
scholarrs863225468
googlers863225468
pharmgkbrs863225468
gwascentralrs863225468
openSNPrs863225468
23andMers863225468
23andMe allrs863225468
SNP Nexus

SNPshotrs863225468
SNPdbers863225468
MSV3drs863225468
GWAS Ctlgrs863225468
Max Magnitude0
ClinVar
Risk rs863225468(C;C)
Alt rs863225468(C;C)
Reference rs863225468(T;T)
Significance Pathogenic
Disease Stomatocytosis I
Variation info
Gene RHAG
CLNDBN Stomatocytosis I
Reversed 1
HGVS NC_000006.11:g.49587039A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000202428.1,