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rs878854344

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854344(-;-)
Make rs878854344(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position176094532
GeneHOXD13
is asnp
is mentioned by
dbSNPrs878854344
ebirs878854344
HLIrs878854344
Exacrs878854344
Varsomers878854344
Maprs878854344
PheGenIrs878854344
hapmaprs878854344
1000 genomesrs878854344
hgdprs878854344
ensemblrs878854344
gopubmedrs878854344
geneviewrs878854344
scholarrs878854344
googlers878854344
pharmgkbrs878854344
gwascentralrs878854344
openSNPrs878854344
23andMers878854344
23andMe allrs878854344
SNP Nexus

SNPshotrs878854344
SNPdbers878854344
MSV3drs878854344
GWAS Ctlgrs878854344
Max Magnitude0
ClinVar
Risk rs878854344(;)
Alt rs878854344(;)
Reference rs878854344(G;G)
Significance Pathogenic
Disease Synpolydactyly 1
Variation info
Gene HOXD13
CLNDBN Synpolydactyly 1
Reversed 0
HGVS NC_000002.11:g.176959260delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000015994.25,