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rs606231153

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231153(C;T)
Make rs606231153(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position156791480
GeneLMBR1
is asnp
is mentioned by
dbSNPrs606231153
ebirs606231153
HLIrs606231153
Exacrs606231153
Varsomers606231153
Maprs606231153
PheGenIrs606231153
hapmaprs606231153
1000 genomesrs606231153
hgdprs606231153
ensemblrs606231153
gopubmedrs606231153
geneviewrs606231153
scholarrs606231153
googlers606231153
pharmgkbrs606231153
gwascentralrs606231153
openSNPrs606231153
23andMers606231153
23andMe allrs606231153
SNP Nexus

SNPshotrs606231153
SNPdbers606231153
MSV3drs606231153
GWAS Ctlgrs606231153
Max Magnitude0
ClinVar
Risk rs606231153(T;T)
Alt rs606231153(T;T)
Reference rs606231153(C;C)
Significance Pathogenic
Disease Polydactyly
Variation info
Gene LMBR1
CLNDBN Polydactyly, preaxial II
Reversed 1
HGVS NC_000007.13:g.156584174G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005189.5,