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rs745990956

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs745990956(A;A)
Make rs745990956(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome20
Position25300853
GeneABHD12
is asnp
is mentioned by
dbSNPrs745990956
ebirs745990956
HLIrs745990956
Exacrs745990956
Varsomers745990956
Maprs745990956
PheGenIrs745990956
hapmaprs745990956
1000 genomesrs745990956
hgdprs745990956
ensemblrs745990956
gopubmedrs745990956
geneviewrs745990956
scholarrs745990956
googlers745990956
pharmgkbrs745990956
gwascentralrs745990956
openSNPrs745990956
23andMers745990956
23andMe allrs745990956
SNP Nexus

SNPshotrs745990956
SNPdbers745990956
MSV3drs745990956
GWAS Ctlgrs745990956
Max Magnitude0
ClinVar
Risk rs745990956(A;A)
Alt rs745990956(A;A)
Reference rs745990956(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABHD12
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.25281489G>A
CLNSRC
CLNACC RCV000171343.1,