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rs552865793

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs552865793(A;A)
Make rs552865793(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position39665814
GeneTCAP
is asnp
is mentioned by
dbSNPrs552865793
ebirs552865793
HLIrs552865793
Exacrs552865793
Varsomers552865793
Maprs552865793
PheGenIrs552865793
hapmaprs552865793
1000 genomesrs552865793
hgdprs552865793
ensemblrs552865793
gopubmedrs552865793
geneviewrs552865793
scholarrs552865793
googlers552865793
pharmgkbrs552865793
gwascentralrs552865793
openSNPrs552865793
23andMers552865793
23andMe allrs552865793
SNP Nexus

SNPshotrs552865793
SNPdbers552865793
MSV3drs552865793
GWAS Ctlgrs552865793
Max Magnitude0
ClinVar
Risk rs552865793(A;A)
Alt rs552865793(A;A)
Reference rs552865793(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TCAP
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.37822067G>A
CLNSRC
CLNACC RCV000183928.2,