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rs606231152

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs606231152(C;C)
Make rs606231152(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position156791581
GeneLMBR1
is asnp
is mentioned by
dbSNPrs606231152
ebirs606231152
HLIrs606231152
Exacrs606231152
Varsomers606231152
Maprs606231152
PheGenIrs606231152
hapmaprs606231152
1000 genomesrs606231152
hgdprs606231152
ensemblrs606231152
gopubmedrs606231152
geneviewrs606231152
scholarrs606231152
googlers606231152
pharmgkbrs606231152
gwascentralrs606231152
openSNPrs606231152
23andMers606231152
23andMe allrs606231152
SNP Nexus

SNPshotrs606231152
SNPdbers606231152
MSV3drs606231152
GWAS Ctlgrs606231152
Max Magnitude0
ClinVar
Risk rs606231152(C;C)
Alt rs606231152(C;C)
Reference rs606231152(T;T)
Significance Pathogenic
Disease Triphalangeal thumb Polydactyly
Variation info
Gene LMBR1
CLNDBN Triphalangeal thumb Polydactyly, preaxial II
Reversed 1
HGVS NC_000007.13:g.156584275A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000005187.3, RCV000005188.3,