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rs150840924

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs150840924(C;T)
Make rs150840924(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156136359
GeneLMNA
is asnp
is mentioned by
dbSNPrs150840924
ebirs150840924
HLIrs150840924
Exacrs150840924
Varsomers150840924
Maprs150840924
PheGenIrs150840924
hapmaprs150840924
1000 genomesrs150840924
hgdprs150840924
ensemblrs150840924
gopubmedrs150840924
geneviewrs150840924
scholarrs150840924
googlers150840924
pharmgkbrs150840924
gwascentralrs150840924
openSNPrs150840924
23andMers150840924
23andMe allrs150840924
SNP Nexus

SNPshotrs150840924
SNPdbers150840924
MSV3drs150840924
GWAS Ctlgrs150840924
Max Magnitude0
ClinVar
Risk rs150840924(T;T)
Alt rs150840924(T;T)
Reference rs150840924(C;C)
Significance Other
Disease not provided Primary dilated cardiomyopathy Hutchinson-Gilford syndrome
Variation info
Gene LMNA
CLNDBN not provided Primary dilated cardiomyopathy Hutchinson-Gilford syndrome
Reversed 0
HGVS NC_000001.10:g.156106150C>T
CLNSRC
CLNACC RCV000057265.1, RCV000148606.2, RCV000150953.2,