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

rs267607600

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607600(A;G)
Make rs267607600(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position156136919
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607600
ebirs267607600
HLIrs267607600
Exacrs267607600
Varsomers267607600
Maprs267607600
PheGenIrs267607600
hapmaprs267607600
1000 genomesrs267607600
hgdprs267607600
ensemblrs267607600
gopubmedrs267607600
geneviewrs267607600
scholarrs267607600
googlers267607600
pharmgkbrs267607600
gwascentralrs267607600
openSNPrs267607600
23andMers267607600
23andMe allrs267607600
SNP Nexus

SNPshotrs267607600
SNPdbers267607600
MSV3drs267607600
GWAS Ctlgrs267607600
Max Magnitude0
ClinVar
Risk rs267607600(G;G)
Alt rs267607600(G;G)
Reference rs267607600(A;A)
Significance Probable-Pathogenic
Disease Congenital muscular dystrophy not provided
Variation info
Gene LMNA
CLNDBN Congenital muscular dystrophy, LMNA-related not provided
Reversed 0
HGVS NC_000001.10:g.156106710A>G
CLNSRC ClinVar Epithelial Biology
CLNACC RCV000030147.1, RCV000057284.1,