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rs606231149

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs606231149(C;C)
Make rs606231149(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position156791547
GeneLMBR1
is asnp
is mentioned by
dbSNPrs606231149
ebirs606231149
HLIrs606231149
Exacrs606231149
Varsomers606231149
Maprs606231149
PheGenIrs606231149
hapmaprs606231149
1000 genomesrs606231149
hgdprs606231149
ensemblrs606231149
gopubmedrs606231149
geneviewrs606231149
scholarrs606231149
googlers606231149
pharmgkbrs606231149
gwascentralrs606231149
openSNPrs606231149
23andMers606231149
23andMe allrs606231149
SNP Nexus

SNPshotrs606231149
SNPdbers606231149
MSV3drs606231149
GWAS Ctlgrs606231149
Max Magnitude0
ClinVar
Risk rs606231149(C;C)
Alt rs606231149(C;C)
Reference rs606231149(T;T)
Significance Pathogenic
Disease Polydactyly Triphalangeal thumb
Variation info
Gene LMBR1
CLNDBN Polydactyly, preaxial II Triphalangeal thumb
Reversed 1
HGVS NC_000007.13:g.156584241A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000005178.3, RCV000005179.3,