Have questions? Visit https://www.reddit.com/r/SNPedia

rs606231147

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231147(A;A)
Make rs606231147(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position156791472
GeneLMBR1
is asnp
is mentioned by
dbSNPrs606231147
ebirs606231147
HLIrs606231147
Exacrs606231147
Varsomers606231147
Maprs606231147
PheGenIrs606231147
hapmaprs606231147
1000 genomesrs606231147
hgdprs606231147
ensemblrs606231147
gopubmedrs606231147
geneviewrs606231147
scholarrs606231147
googlers606231147
pharmgkbrs606231147
gwascentralrs606231147
openSNPrs606231147
23andMers606231147
23andMe allrs606231147
SNP Nexus

SNPshotrs606231147
SNPdbers606231147
MSV3drs606231147
GWAS Ctlgrs606231147
Max Magnitude0
ClinVar
Risk rs606231147(A;A)
Alt rs606231147(A;A)
Reference rs606231147(G;G)
Significance Pathogenic
Disease Tibia
Variation info
Gene LMBR1
CLNDBN Tibia, hypoplasia or aplasia of, with polydactyly
Reversed 1
HGVS NC_000007.13:g.156584166C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005176.4,