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rs878854400

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878854400(C;T)
Make rs878854400(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position176093632
GeneHOXD13
is asnp
is mentioned by
dbSNPrs878854400
ebirs878854400
HLIrs878854400
Exacrs878854400
Varsomers878854400
Maprs878854400
PheGenIrs878854400
hapmaprs878854400
1000 genomesrs878854400
hgdprs878854400
ensemblrs878854400
gopubmedrs878854400
geneviewrs878854400
scholarrs878854400
googlers878854400
pharmgkbrs878854400
gwascentralrs878854400
openSNPrs878854400
23andMers878854400
23andMe allrs878854400
SNP Nexus

SNPshotrs878854400
SNPdbers878854400
MSV3drs878854400
GWAS Ctlgrs878854400
Max Magnitude0
ClinVar
Risk rs878854400(T;T)
Alt rs878854400(T;T)
Reference rs878854400(C;C)
Significance Pathogenic
Disease Synpolydactyly 1
Variation info
Gene HOXD13
CLNDBN Synpolydactyly 1
Reversed 0
HGVS NC_000002.11:g.176958360C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000210952.2,