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rs863225469

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225469(G;G)
Make rs863225469(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position49619338
GeneRHAG
is asnp
is mentioned by
dbSNPrs863225469
ebirs863225469
HLIrs863225469
Exacrs863225469
Varsomers863225469
Maprs863225469
PheGenIrs863225469
hapmaprs863225469
1000 genomesrs863225469
hgdprs863225469
ensemblrs863225469
gopubmedrs863225469
geneviewrs863225469
scholarrs863225469
googlers863225469
pharmgkbrs863225469
gwascentralrs863225469
openSNPrs863225469
23andMers863225469
23andMe allrs863225469
SNP Nexus

SNPshotrs863225469
SNPdbers863225469
MSV3drs863225469
GWAS Ctlgrs863225469
Max Magnitude0
ClinVar
Risk rs863225469(G;G)
Alt rs863225469(G;G)
Reference rs863225469(T;T)
Significance Pathogenic
Disease Stomatocytosis I
Variation info
Gene RHAG
CLNDBN Stomatocytosis I
Reversed 1
HGVS NC_000006.11:g.49587051A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000202426.2,