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rs875989842

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs875989842(A;A)
Make rs875989842(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position176094671
GeneHOXD13
is asnp
is mentioned by
dbSNPrs875989842
ebirs875989842
HLIrs875989842
Exacrs875989842
Varsomers875989842
Maprs875989842
PheGenIrs875989842
hapmaprs875989842
1000 genomesrs875989842
hgdprs875989842
ensemblrs875989842
gopubmedrs875989842
geneviewrs875989842
scholarrs875989842
googlers875989842
pharmgkbrs875989842
gwascentralrs875989842
openSNPrs875989842
23andMers875989842
23andMe allrs875989842
SNP Nexus

SNPshotrs875989842
SNPdbers875989842
MSV3drs875989842
GWAS Ctlgrs875989842
Max Magnitude0
ClinVar
Risk rs875989842(A;A)
Alt rs875989842(A;A)
Reference rs875989842(C;C)
Significance Pathogenic
Disease BRACHYDACTYLY-SYNDACTYLY-OLIGODACTYLY SYNDROME (1 patient)
Variation info
Gene HOXD13
CLNDBN BRACHYDACTYLY-SYNDACTYLY-OLIGODACTYLY SYNDROME (1 patient)
Reversed 0
HGVS NC_000002.11:g.176959399C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000210948.2,