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rs148360332

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs148360332(C;T)
Make rs148360332(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position77453359
GeneVIPAS39
is asnp
is mentioned by
dbSNPrs148360332
ebirs148360332
HLIrs148360332
Exacrs148360332
Varsomers148360332
Maprs148360332
PheGenIrs148360332
hapmaprs148360332
1000 genomesrs148360332
hgdprs148360332
ensemblrs148360332
gopubmedrs148360332
geneviewrs148360332
scholarrs148360332
googlers148360332
pharmgkbrs148360332
gwascentralrs148360332
openSNPrs148360332
23andMers148360332
23andMe allrs148360332
SNP Nexus

SNPshotrs148360332
SNPdbers148360332
MSV3drs148360332
GWAS Ctlgrs148360332
Max Magnitude0
ClinVar
Risk rs148360332(T;T)
Alt rs148360332(T;T)
Reference rs148360332(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene VIPAS39
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.77919702C>T
CLNSRC
CLNACC RCV000171225.1,