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rs780787386

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs780787386(C;G)
Make rs780787386(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position7695497
GeneGDF3
is asnp
is mentioned by
dbSNPrs780787386
ebirs780787386
HLIrs780787386
Exacrs780787386
Varsomers780787386
Maprs780787386
PheGenIrs780787386
hapmaprs780787386
1000 genomesrs780787386
hgdprs780787386
ensemblrs780787386
gopubmedrs780787386
geneviewrs780787386
scholarrs780787386
googlers780787386
pharmgkbrs780787386
gwascentralrs780787386
openSNPrs780787386
23andMers780787386
23andMe allrs780787386
SNP Nexus

SNPshotrs780787386
SNPdbers780787386
MSV3drs780787386
GWAS Ctlgrs780787386
Max Magnitude0
ClinVar
Risk rs780787386(G,T;G,T)
Alt rs780787386(G,T;G,T)
Reference rs780787386(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GDF3
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.7848093C>G
CLNSRC
CLNACC RCV000171205.1,