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rs753744791

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs753744791(A;A)
Make rs753744791(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position39665828
GeneTCAP
is asnp
is mentioned by
dbSNPrs753744791
ebirs753744791
HLIrs753744791
Exacrs753744791
Varsomers753744791
Maprs753744791
PheGenIrs753744791
hapmaprs753744791
1000 genomesrs753744791
hgdprs753744791
ensemblrs753744791
gopubmedrs753744791
geneviewrs753744791
scholarrs753744791
googlers753744791
pharmgkbrs753744791
gwascentralrs753744791
openSNPrs753744791
23andMers753744791
23andMe allrs753744791
SNP Nexus

SNPshotrs753744791
SNPdbers753744791
MSV3drs753744791
GWAS Ctlgrs753744791
Max Magnitude0
ClinVar
Risk rs753744791(A;A)
Alt rs753744791(A;A)
Reference rs753744791(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TCAP
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.37822081G>A
CLNSRC
CLNACC RCV000183929.1,