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rs104893635

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104893635(A;G)
Make rs104893635(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position176094672
GeneHOXD13
is asnp
is mentioned by
dbSNPrs104893635
ebirs104893635
HLIrs104893635
Exacrs104893635
Varsomers104893635
Maprs104893635
PheGenIrs104893635
hapmaprs104893635
1000 genomesrs104893635
hgdprs104893635
ensemblrs104893635
gopubmedrs104893635
geneviewrs104893635
scholarrs104893635
googlers104893635
pharmgkbrs104893635
gwascentralrs104893635
openSNPrs104893635
23andMers104893635
23andMe allrs104893635
SNP Nexus

SNPshotrs104893635
SNPdbers104893635
MSV3drs104893635
GWAS Ctlgrs104893635
Max Magnitude0
OMIM142989
Desc
Variant0009
Relatedalso
ClinVar
Risk rs104893635(G;G)
Alt rs104893635(G;G)
Reference rs104893635(A;A)
Significance Pathogenic
Disease Syndactyly
Variation info
Gene HOXD13
CLNDBN Syndactyly, type V
Reversed 0
HGVS NC_000002.11:g.176959400A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000016002.26,