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rs775933965

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs775933965(A;A)
Make rs775933965(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position45366406
GeneGATM
is asnp
is mentioned by
dbSNPrs775933965
ebirs775933965
HLIrs775933965
Exacrs775933965
Varsomers775933965
Maprs775933965
PheGenIrs775933965
hapmaprs775933965
1000 genomesrs775933965
hgdprs775933965
ensemblrs775933965
gopubmedrs775933965
geneviewrs775933965
scholarrs775933965
googlers775933965
pharmgkbrs775933965
gwascentralrs775933965
openSNPrs775933965
23andMers775933965
23andMe allrs775933965
SNP Nexus

SNPshotrs775933965
SNPdbers775933965
MSV3drs775933965
GWAS Ctlgrs775933965
Max Magnitude0
ClinVar
Risk rs775933965(A;A)
Alt rs775933965(A;A)
Reference rs775933965(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene GATM
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.45658604G>A
CLNSRC
CLNACC RCV000187602.1,