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rs606231231

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs606231231(G;G)
Make rs606231231(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position156791542
GeneLMBR1
is asnp
is mentioned by
dbSNPrs606231231
ebirs606231231
HLIrs606231231
Exacrs606231231
Varsomers606231231
Maprs606231231
PheGenIrs606231231
hapmaprs606231231
1000 genomesrs606231231
hgdprs606231231
ensemblrs606231231
gopubmedrs606231231
geneviewrs606231231
scholarrs606231231
googlers606231231
pharmgkbrs606231231
gwascentralrs606231231
openSNPrs606231231
23andMers606231231
23andMe allrs606231231
SNP Nexus

SNPshotrs606231231
SNPdbers606231231
MSV3drs606231231
GWAS Ctlgrs606231231
Max Magnitude0
ClinVar
Risk rs606231231(G;G)
Alt rs606231231(G;G)
Reference rs606231231(T;T)
Significance Pathogenic
Disease Polydactyly
Variation info
Gene LMBR1
CLNDBN Polydactyly, preaxial II
Reversed 1
HGVS NC_000007.13:g.156584236A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023454.5,