Have questions? Visit https://www.reddit.com/r/SNPedia

rs797044433

From SNPedia

Orientationminus
Make rs797044433(-;-)
Make rs797044433(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position72345462
GeneHEXA
is asnp
is mentioned by
dbSNPrs797044433
ebirs797044433
HLIrs797044433
Exacrs797044433
Varsomers797044433
Maprs797044433
PheGenIrs797044433
hapmaprs797044433
1000 genomesrs797044433
hgdprs797044433
ensemblrs797044433
gopubmedrs797044433
geneviewrs797044433
scholarrs797044433
googlers797044433
pharmgkbrs797044433
gwascentralrs797044433
openSNPrs797044433
23andMers797044433
23andMe allrs797044433
SNP Nexus

SNPshotrs797044433
SNPdbers797044433
MSV3drs797044433
GWAS Ctlgrs797044433
Max Magnitude
ClinVar
Risk rs797044433(;)
Alt rs797044433(;)
Reference rs797044433(C;C)
Significance Pathogenic
Disease Tay-Sachs disease
Variation info
Gene HEXA
CLNDBN Tay-Sachs disease
Reversed 1
HGVS NC_000015.9:g.72637803delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000004098.2,