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rs370717845

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs370717845(A;A)
Make rs370717845(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position43161462
GeneHGSNAT
is asnp
is mentioned by
dbSNPrs370717845
ebirs370717845
HLIrs370717845
Exacrs370717845
Varsomers370717845
Maprs370717845
PheGenIrs370717845
hapmaprs370717845
1000 genomesrs370717845
hgdprs370717845
ensemblrs370717845
gopubmedrs370717845
geneviewrs370717845
scholarrs370717845
googlers370717845
pharmgkbrs370717845
gwascentralrs370717845
openSNPrs370717845
23andMers370717845
23andMe allrs370717845
SNP Nexus

SNPshotrs370717845
SNPdbers370717845
MSV3drs370717845
GWAS Ctlgrs370717845
Max Magnitude0
ClinVar
Risk rs370717845(A;A)
Alt rs370717845(A;A)
Reference rs370717845(G;G)
Significance Pathogenic
Disease Mucopolysaccharidosis
Variation info
Gene HGSNAT
CLNDBN Mucopolysaccharidosis, MPS-III-C
Reversed 0
HGVS NC_000008.10:g.43016605G>A
CLNSRC
CLNACC RCV000239404.1,