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rs539275646

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs539275646(C;T)
Make rs539275646(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position144055135
GeneOPLAH
is asnp
is mentioned by
dbSNPrs539275646
ebirs539275646
HLIrs539275646
Exacrs539275646
Varsomers539275646
Maprs539275646
PheGenIrs539275646
hapmaprs539275646
1000 genomesrs539275646
hgdprs539275646
ensemblrs539275646
gopubmedrs539275646
geneviewrs539275646
scholarrs539275646
googlers539275646
pharmgkbrs539275646
gwascentralrs539275646
openSNPrs539275646
23andMers539275646
23andMe allrs539275646
SNP Nexus

SNPshotrs539275646
SNPdbers539275646
MSV3drs539275646
GWAS Ctlgrs539275646
Max Magnitude0
ClinVar
Risk rs539275646(T;T)
Alt rs539275646(T;T)
Reference rs539275646(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OPLAH
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.145110038C>T
CLNSRC
CLNACC RCV000171537.1,