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rs764838478

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs764838478(-;-)
Make rs764838478(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position176094478
GeneHOXD13
is asnp
is mentioned by
dbSNPrs764838478
ebirs764838478
HLIrs764838478
Exacrs764838478
Varsomers764838478
Maprs764838478
PheGenIrs764838478
hapmaprs764838478
1000 genomesrs764838478
hgdprs764838478
ensemblrs764838478
gopubmedrs764838478
geneviewrs764838478
scholarrs764838478
googlers764838478
pharmgkbrs764838478
gwascentralrs764838478
openSNPrs764838478
23andMers764838478
23andMe allrs764838478
SNP Nexus

SNPshotrs764838478
SNPdbers764838478
MSV3drs764838478
GWAS Ctlgrs764838478
Max Magnitude0
ClinVar
Risk rs764838478(;)
Alt rs764838478(;)
Reference rs764838478(A;A)
Significance Pathogenic
Disease Synpolydactyly 1
Variation info
Gene HOXD13
CLNDBN Synpolydactyly 1
Reversed 0
HGVS NC_000002.11:g.176959206delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000015999.21,