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rs201317502

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201317502(C;G)
Make rs201317502(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position45420648
GenePIGT
is asnp
is mentioned by
dbSNPrs201317502
dbSNP (old)rs201317502
ClinGenrs201317502
ebirs201317502
HLIrs201317502
Exacrs201317502
Gnomadrs201317502
Varsomers201317502
Maprs201317502
PheGenIrs201317502
Biobankrs201317502
1000 genomesrs201317502
hgdprs201317502
ensemblrs201317502
gopubmedrs201317502
geneviewrs201317502
scholarrs201317502
googlers201317502
pharmgkbrs201317502
gwascentralrs201317502
openSNPrs201317502
23andMers201317502
23andMe allrs201317502
SNPshotrs201317502
SNPdbers201317502
MSV3drs201317502
GWAS Ctlgrs201317502
Max Magnitude0
ClinVar
Risk rs201317502(G;G) rs201317502(T;T)
Alt rs201317502(G;G) rs201317502(T;T)
Reference Rs201317502(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PIGT
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.44049288C>T
CLNSRC
CLNACC RCV000414606.1,