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rs200639270

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200639270(A;A)
Make rs200639270(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position12893543
GeneGCDH
is asnp
is mentioned by
dbSNPrs200639270
dbSNP (old)rs200639270
ClinGenrs200639270
ebirs200639270
HLIrs200639270
Exacrs200639270
Gnomadrs200639270
Varsomers200639270
Maprs200639270
PheGenIrs200639270
Biobankrs200639270
1000 genomesrs200639270
hgdprs200639270
ensemblrs200639270
gopubmedrs200639270
geneviewrs200639270
scholarrs200639270
googlers200639270
pharmgkbrs200639270
gwascentralrs200639270
openSNPrs200639270
23andMers200639270
23andMe allrs200639270
SNPshotrs200639270
SNPdbers200639270
MSV3drs200639270
GWAS Ctlgrs200639270
Max Magnitude0
ClinVar
Risk rs200639270(A;A)
Alt rs200639270(A;A)
Reference Rs200639270(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene GCDH
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.13004357G>A
CLNSRC
CLNACC RCV000444441.1,