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

rs771937610

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs771937610(A;A)
Make rs771937610(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position130494984
GeneASS1, LOC105376294
is asnp
is mentioned by
dbSNPrs771937610
ebirs771937610
HLIrs771937610
Exacrs771937610
Varsomers771937610
Maprs771937610
PheGenIrs771937610
hapmaprs771937610
1000 genomesrs771937610
hgdprs771937610
ensemblrs771937610
gopubmedrs771937610
geneviewrs771937610
scholarrs771937610
googlers771937610
pharmgkbrs771937610
gwascentralrs771937610
openSNPrs771937610
23andMers771937610
23andMe allrs771937610
SNP Nexus

SNPshotrs771937610
SNPdbers771937610
MSV3drs771937610
GWAS Ctlgrs771937610
Max Magnitude0
ClinVar
Risk rs771937610(A;A)
Alt rs771937610(A;A)
Reference rs771937610(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ASS1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.133370371G>A
CLNSRC
CLNACC RCV000185788.2,