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rs794729178

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729178(G;T)
Make rs794729178(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position39665474
GeneTCAP
is asnp
is mentioned by
dbSNPrs794729178
ebirs794729178
HLIrs794729178
Exacrs794729178
Varsomers794729178
Maprs794729178
PheGenIrs794729178
hapmaprs794729178
1000 genomesrs794729178
hgdprs794729178
ensemblrs794729178
gopubmedrs794729178
geneviewrs794729178
scholarrs794729178
googlers794729178
pharmgkbrs794729178
gwascentralrs794729178
openSNPrs794729178
23andMers794729178
23andMe allrs794729178
SNP Nexus

SNPshotrs794729178
SNPdbers794729178
MSV3drs794729178
GWAS Ctlgrs794729178
Max Magnitude0
ClinVar
Risk rs794729178(T;T)
Alt rs794729178(T;T)
Reference rs794729178(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TCAP
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.37821727G>T
CLNSRC
CLNACC RCV000183932.1,