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rs777518512

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs777518512(C;T)
Make rs777518512(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position39665864
GeneTCAP
is asnp
is mentioned by
dbSNPrs777518512
ebirs777518512
HLIrs777518512
Exacrs777518512
Varsomers777518512
Maprs777518512
PheGenIrs777518512
hapmaprs777518512
1000 genomesrs777518512
hgdprs777518512
ensemblrs777518512
gopubmedrs777518512
geneviewrs777518512
scholarrs777518512
googlers777518512
pharmgkbrs777518512
gwascentralrs777518512
openSNPrs777518512
23andMers777518512
23andMe allrs777518512
SNP Nexus

SNPshotrs777518512
SNPdbers777518512
MSV3drs777518512
GWAS Ctlgrs777518512
Max Magnitude0
ClinVar
Risk rs777518512(T;T)
Alt rs777518512(T;T)
Reference rs777518512(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TCAP
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.37822117C>T
CLNSRC
CLNACC RCV000183919.2,