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rs758503371

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs758503371(C;T)
Make rs758503371(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position12896333
GeneGCDH
is asnp
is mentioned by
dbSNPrs758503371
dbSNP (classic)rs758503371
ClinGenrs758503371
ebirs758503371
HLIrs758503371
Exacrs758503371
Gnomadrs758503371
Varsomers758503371
LitVarrs758503371
Maprs758503371
PheGenIrs758503371
Biobankrs758503371
1000 genomesrs758503371
hgdprs758503371
ensemblrs758503371
geneviewrs758503371
scholarrs758503371
googlers758503371
pharmgkbrs758503371
gwascentralrs758503371
openSNPrs758503371
23andMers758503371
SNPshotrs758503371
SNPdbers758503371
MSV3drs758503371
GWAS Ctlgrs758503371
Max Magnitude0
ClinVar
Risk rs758503371(T;T)
Alt rs758503371(T;T)
Reference Rs758503371(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GCDH
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.13007147C>T
CLNSRC
CLNACC RCV000416219.1,