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rs59267781

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs59267781(C;G)
Make rs59267781(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156138657
GeneLMNA
is asnp
is mentioned by
dbSNPrs59267781
ebirs59267781
HLIrs59267781
Exacrs59267781
Varsomers59267781
Maprs59267781
PheGenIrs59267781
hapmaprs59267781
1000 genomesrs59267781
hgdprs59267781
ensemblrs59267781
gopubmedrs59267781
geneviewrs59267781
scholarrs59267781
googlers59267781
pharmgkbrs59267781
gwascentralrs59267781
openSNPrs59267781
23andMers59267781
23andMe allrs59267781
SNP Nexus

SNPshotrs59267781
SNPdbers59267781
MSV3drs59267781
GWAS Ctlgrs59267781
Max Magnitude0
ClinVar
Risk rs59267781(G;G)
Alt rs59267781(G;G)
Reference rs59267781(C;C)
Significance Pathogenic
Disease not provided Hutchinson-Gilford syndrome
Variation info
Gene LMNA
CLNDBN not provided Hutchinson-Gilford syndrome
Reversed 0
HGVS NC_000001.10:g.156108448C>G
CLNSRC
CLNACC RCV000057366.1, RCV000192021.1,