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rs431905505

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs431905505(C;C)
Make rs431905505(C;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position19973664
GeneWDR35
is asnp
is mentioned by
dbSNPrs431905505
ebirs431905505
HLIrs431905505
Exacrs431905505
Varsomers431905505
Maprs431905505
PheGenIrs431905505
hapmaprs431905505
1000 genomesrs431905505
hgdprs431905505
ensemblrs431905505
gopubmedrs431905505
geneviewrs431905505
scholarrs431905505
googlers431905505
pharmgkbrs431905505
gwascentralrs431905505
openSNPrs431905505
23andMers431905505
23andMe allrs431905505
SNP Nexus

SNPshotrs431905505
SNPdbers431905505
MSV3drs431905505
GWAS Ctlgrs431905505
Max Magnitude0
ClinVar
Risk rs431905505(C;C)
Alt rs431905505(C;C)
Reference rs431905505(T;T)
Significance Pathogenic
Disease Short rib polydactyly syndrome 5
Variation info
Gene WDR35
CLNDBN Short rib polydactyly syndrome 5
Reversed 1
HGVS NC_000002.11:g.20173425A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000024039.4,