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

rs397509415

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509415(A;G)
Make rs397509415(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position18059568
GeneASAH1
is asnp
is mentioned by
dbSNPrs397509415
ebirs397509415
HLIrs397509415
Exacrs397509415
Varsomers397509415
Maprs397509415
PheGenIrs397509415
hapmaprs397509415
1000 genomesrs397509415
hgdprs397509415
ensemblrs397509415
gopubmedrs397509415
geneviewrs397509415
scholarrs397509415
googlers397509415
pharmgkbrs397509415
gwascentralrs397509415
openSNPrs397509415
23andMers397509415
23andMe allrs397509415
SNP Nexus

SNPshotrs397509415
SNPdbers397509415
MSV3drs397509415
GWAS Ctlgrs397509415
Max Magnitude0
ClinVar
Risk rs397509415(G;G)
Alt rs397509415(G;G)
Reference rs397509415(A;A)
Significance Pathogenic
Disease Farber's lipogranulomatosis
Variation info
Gene ASAH1
CLNDBN Farber's lipogranulomatosis
Reversed 1
HGVS NC_000008.10:g.17917077T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000049322.5,