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rs756455049

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs756455049(A;G)
Make rs756455049(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position18062422
GeneASAH1
is asnp
is mentioned by
dbSNPrs756455049
ebirs756455049
HLIrs756455049
Exacrs756455049
Varsomers756455049
Maprs756455049
PheGenIrs756455049
hapmaprs756455049
1000 genomesrs756455049
hgdprs756455049
ensemblrs756455049
gopubmedrs756455049
geneviewrs756455049
scholarrs756455049
googlers756455049
pharmgkbrs756455049
gwascentralrs756455049
openSNPrs756455049
23andMers756455049
23andMe allrs756455049
SNP Nexus

SNPshotrs756455049
SNPdbers756455049
MSV3drs756455049
GWAS Ctlgrs756455049
Max Magnitude0
ClinVar
Risk rs756455049(G;G)
Alt rs756455049(G;G)
Reference rs756455049(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ASAH1
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.17919931A>G
CLNSRC
CLNACC RCV000171533.1,