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rs267607582

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607582(G;G)
Make rs267607582(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156137642
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607582
ebirs267607582
HLIrs267607582
Exacrs267607582
Varsomers267607582
Maprs267607582
PheGenIrs267607582
hapmaprs267607582
1000 genomesrs267607582
hgdprs267607582
ensemblrs267607582
gopubmedrs267607582
geneviewrs267607582
scholarrs267607582
googlers267607582
pharmgkbrs267607582
gwascentralrs267607582
openSNPrs267607582
23andMers267607582
23andMe allrs267607582
SNP Nexus

SNPshotrs267607582
SNPdbers267607582
MSV3drs267607582
GWAS Ctlgrs267607582
Max Magnitude0
ClinVar
Risk rs267607582(G;G)
Alt rs267607582(G;G)
Reference rs267607582(T;T)
Significance Pathogenic
Disease Heart-hand syndrome not provided
Variation info
Gene LMNA
CLNDBN Heart-hand syndrome, Slovenian type not provided
Reversed 0
HGVS NC_000001.10:g.156107433T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000015618.26, RCV000057337.1,