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rs878853102

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853102(C;T)
Make rs878853102(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position96160620
GeneGDF6
is asnp
is mentioned by
dbSNPrs878853102
ebirs878853102
HLIrs878853102
Exacrs878853102
Varsomers878853102
Maprs878853102
PheGenIrs878853102
hapmaprs878853102
1000 genomesrs878853102
hgdprs878853102
ensemblrs878853102
gopubmedrs878853102
geneviewrs878853102
scholarrs878853102
googlers878853102
pharmgkbrs878853102
gwascentralrs878853102
openSNPrs878853102
23andMers878853102
23andMe allrs878853102
SNP Nexus

SNPshotrs878853102
SNPdbers878853102
MSV3drs878853102
GWAS Ctlgrs878853102
Max Magnitude0
ClinVar
Risk rs878853102(T;T)
Alt rs878853102(T;T)
Reference rs878853102(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GDF6
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.97172848G>A
CLNSRC
CLNACC RCV000224148.1,