Have questions? Visit https://www.reddit.com/r/SNPedia

rs587776959

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776959(C;T)
Make rs587776959(T;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position373858
GeneZNF141
is asnp
is mentioned by
dbSNPrs587776959
ebirs587776959
HLIrs587776959
Exacrs587776959
Varsomers587776959
Maprs587776959
PheGenIrs587776959
hapmaprs587776959
1000 genomesrs587776959
hgdprs587776959
ensemblrs587776959
gopubmedrs587776959
geneviewrs587776959
scholarrs587776959
googlers587776959
pharmgkbrs587776959
gwascentralrs587776959
openSNPrs587776959
23andMers587776959
23andMe allrs587776959
SNP Nexus

SNPshotrs587776959
SNPdbers587776959
MSV3drs587776959
GWAS Ctlgrs587776959
Max Magnitude0
ClinVar
Risk rs587776959(T;T)
Alt rs587776959(T;T)
Reference rs587776959(C;C)
Significance Other
Disease Postaxial polydactyly type A6
Variation info
Gene ZNF141
CLNDBN Postaxial polydactyly type A6
Reversed 0
HGVS NC_000004.11:g.367647C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000043502.24,