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rs863225434

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225434(A;T)
Make rs863225434(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position72346271
GeneHEXA
is asnp
is mentioned by
dbSNPrs863225434
ebirs863225434
HLIrs863225434
Exacrs863225434
Varsomers863225434
Maprs863225434
PheGenIrs863225434
hapmaprs863225434
1000 genomesrs863225434
hgdprs863225434
ensemblrs863225434
gopubmedrs863225434
geneviewrs863225434
scholarrs863225434
googlers863225434
pharmgkbrs863225434
gwascentralrs863225434
openSNPrs863225434
23andMers863225434
23andMe allrs863225434
SNP Nexus

SNPshotrs863225434
SNPdbers863225434
MSV3drs863225434
GWAS Ctlgrs863225434
Max Magnitude0
ClinVar
Risk rs863225434(T;T)
Alt rs863225434(T;T)
Reference rs863225434(A;A)
Significance Pathogenic
Disease Tay-Sachs disease
Variation info
Gene HEXA
CLNDBN Tay-Sachs disease
Reversed 1
HGVS NC_000015.9:g.72638612T>A
CLNSRC
CLNACC RCV000202369.1,