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rs398122527

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122527(G;T)
Make rs398122527(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position97021048
GeneDLX5
is asnp
is mentioned by
dbSNPrs398122527
ebirs398122527
HLIrs398122527
Exacrs398122527
Varsomers398122527
Maprs398122527
PheGenIrs398122527
hapmaprs398122527
1000 genomesrs398122527
hgdprs398122527
ensemblrs398122527
gopubmedrs398122527
geneviewrs398122527
scholarrs398122527
googlers398122527
pharmgkbrs398122527
gwascentralrs398122527
openSNPrs398122527
23andMers398122527
23andMe allrs398122527
SNP Nexus

SNPshotrs398122527
SNPdbers398122527
MSV3drs398122527
GWAS Ctlgrs398122527
Max Magnitude0
ClinVar
Risk rs398122527(T;T)
Alt rs398122527(T;T)
Reference rs398122527(G;G)
Significance Pathogenic
Disease not provided Split-hand/foot malformation 1
Variation info
Gene DLX5
CLNDBN not provided Split-hand/foot malformation 1
Reversed 1
HGVS NC_000007.13:g.96650360C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000077764.1, RCV000144532.2,