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rs587779405

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779405(-;-)
Make rs587779405(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position151266820
GeneGM2A
is asnp
is mentioned by
dbSNPrs587779405
ebirs587779405
HLIrs587779405
Exacrs587779405
Varsomers587779405
Maprs587779405
PheGenIrs587779405
hapmaprs587779405
1000 genomesrs587779405
hgdprs587779405
ensemblrs587779405
gopubmedrs587779405
geneviewrs587779405
scholarrs587779405
googlers587779405
pharmgkbrs587779405
gwascentralrs587779405
openSNPrs587779405
23andMers587779405
23andMe allrs587779405
SNP Nexus

SNPshotrs587779405
SNPdbers587779405
MSV3drs587779405
GWAS Ctlgrs587779405
Max Magnitude0
ClinVar
Risk rs587779405(;)
Alt rs587779405(;)
Reference rs587779405(C;C)
Significance Pathogenic
Disease Tay-Sachs disease
Variation info
Gene GM2A
CLNDBN Tay-Sachs disease
Reversed 0
HGVS NC_000005.9:g.150646381delC
CLNSRC
CLNACC RCV000087094.1,