rs153478

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs153478(A;G)

Make rs153478(G;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

151259878

Gene

GM2A

is a	snp
is	mentioned by
dbSNP	rs153478
dbSNP (classic)	rs153478
ClinGen	rs153478
ebi	rs153478
HLI	rs153478
Exac	rs153478
Gnomad	rs153478
Varsome	rs153478
LitVar	rs153478
Map	rs153478
PheGenI	rs153478
Biobank	rs153478
1000 genomes	rs153478
hgdp	rs153478
ensembl	rs153478
geneview	rs153478
scholar	rs153478
google	rs153478
pharmgkb	rs153478
gwascentral	rs153478
openSNP	rs153478
23andMe	rs153478
SNPshot	rs153478
SNPdbe	rs153478
MSV3d	rs153478
GWAS Ctlg	rs153478

GMAF

0.185

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

ClinVar
Risk	rs153478(G;G)
Alt	rs153478(G;G)
Reference	Rs153478(A;A)
Significance	Non-pathogenic
Disease	not specified Tay-Sachs disease
Variation	info
Gene	GM2A
CLNDBN	not specified Tay-Sachs disease, variant AB
Reversed	0
HGVS	NC_000005.9:g.150639439A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000153333.4, RCV000286625.1,