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rs886039878

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039878(A;A)
Make rs886039878(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome20
Position35434018
GeneGDF5
is asnp
is mentioned by
dbSNPrs886039878
dbSNP (classic)rs886039878
ClinGenrs886039878
ebirs886039878
HLIrs886039878
Exacrs886039878
Gnomadrs886039878
Varsomers886039878
LitVarrs886039878
Maprs886039878
PheGenIrs886039878
Biobankrs886039878
1000 genomesrs886039878
hgdprs886039878
ensemblrs886039878
geneviewrs886039878
scholarrs886039878
googlers886039878
pharmgkbrs886039878
gwascentralrs886039878
openSNPrs886039878
23andMers886039878
23andMe allrs886039878
SNPshotrs886039878
SNPdbers886039878
MSV3drs886039878
GWAS Ctlgrs886039878
Max Magnitude0
ClinVar
Risk rs886039878(A;A)
Alt rs886039878(A;A)
Reference Rs886039878(G;G)
Significance Probable-Pathogenic
Disease Brachydactyly type C
Variation info
Gene GDF5
CLNDBN Brachydactyly type C
Reversed 1
HGVS NC_000020.10:g.34021816C>T
CLNSRC
CLNACC RCV000256400.1,