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rs104893634

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104893634(A;A)
Make rs104893634(A;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position176119164
GeneHOXD10
is asnp
is mentioned by
dbSNPrs104893634
ebirs104893634
HLIrs104893634
Exacrs104893634
Varsomers104893634
Maprs104893634
PheGenIrs104893634
hapmaprs104893634
1000 genomesrs104893634
hgdprs104893634
ensemblrs104893634
gopubmedrs104893634
geneviewrs104893634
scholarrs104893634
googlers104893634
pharmgkbrs104893634
gwascentralrs104893634
openSNPrs104893634
23andMers104893634
23andMe allrs104893634
SNP Nexus

SNPshotrs104893634
SNPdbers104893634
MSV3drs104893634
GWAS Ctlgrs104893634
Max Magnitude0
OMIM142984
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104893634(A;A)
Alt rs104893634(A;A)
Reference rs104893634(T;T)
Significance Pathogenic
Disease Vertical talus
Variation info
Gene HOXD10
CLNDBN Vertical talus, congenital
Reversed 0
HGVS NC_000002.11:g.176983892T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000016006.26,