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rs536639583

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs536639583(C;C)
Make rs536639583(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position176092922
GeneHOXD13
is asnp
is mentioned by
dbSNPrs536639583
ebirs536639583
HLIrs536639583
Exacrs536639583
Varsomers536639583
Maprs536639583
PheGenIrs536639583
hapmaprs536639583
1000 genomesrs536639583
hgdprs536639583
ensemblrs536639583
gopubmedrs536639583
geneviewrs536639583
scholarrs536639583
googlers536639583
pharmgkbrs536639583
gwascentralrs536639583
openSNPrs536639583
23andMers536639583
23andMe allrs536639583
SNP Nexus

SNPshotrs536639583
SNPdbers536639583
MSV3drs536639583
GWAS Ctlgrs536639583
Max Magnitude0
ClinVar
Risk rs536639583(C;C)
Alt rs536639583(C;C)
Reference rs536639583(G;G)
Significance Pathogenic
Disease Synpolydactyly 1
Variation info
Gene HOXD13
CLNDBN Synpolydactyly 1
Reversed 0
HGVS NC_000002.11:g.176957650G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000210944.2,