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rs606231151

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231151(C;G)
Make rs606231151(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position156791255
GeneLMBR1
is asnp
is mentioned by
dbSNPrs606231151
ebirs606231151
HLIrs606231151
Exacrs606231151
Varsomers606231151
Maprs606231151
PheGenIrs606231151
hapmaprs606231151
1000 genomesrs606231151
hgdprs606231151
ensemblrs606231151
gopubmedrs606231151
geneviewrs606231151
scholarrs606231151
googlers606231151
pharmgkbrs606231151
gwascentralrs606231151
openSNPrs606231151
23andMers606231151
23andMe allrs606231151
SNP Nexus

SNPshotrs606231151
SNPdbers606231151
MSV3drs606231151
GWAS Ctlgrs606231151
Max Magnitude0
ClinVar
Risk rs606231151(G;G)
Alt rs606231151(G;G)
Reference rs606231151(C;C)
Significance Pathogenic
Disease Polydactyly Triphalangeal thumb
Variation info
Gene LMBR1
CLNDBN Polydactyly, preaxial II Triphalangeal thumb
Reversed 1
HGVS NC_000007.13:g.156583949G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000005183.3, RCV000005184.3,