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rs587777842

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777842(A;A)
Make rs587777842(A;C)
ReferenceGRCh38 38.1/142
Chromosome7
Position97024509
GeneDLX5
is asnp
is mentioned by
dbSNPrs587777842
ebirs587777842
HLIrs587777842
Exacrs587777842
Varsomers587777842
Maprs587777842
PheGenIrs587777842
hapmaprs587777842
1000 genomesrs587777842
hgdprs587777842
ensemblrs587777842
gopubmedrs587777842
geneviewrs587777842
scholarrs587777842
googlers587777842
pharmgkbrs587777842
gwascentralrs587777842
openSNPrs587777842
23andMers587777842
23andMe allrs587777842
SNP Nexus

SNPshotrs587777842
SNPdbers587777842
MSV3drs587777842
GWAS Ctlgrs587777842
Max Magnitude0
ClinVar
Risk rs587777842(A;A)
Alt rs587777842(A;A)
Reference rs587777842(C;C)
Significance Pathogenic
Disease Split-hand/foot malformation 1
Variation info
Gene DLX5
CLNDBN Split-hand/foot malformation 1
Reversed 0
HGVS NC_000007.13:g.96653821C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144533.2,