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rs797044486

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044486(A;A)
Make rs797044486(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156138560
GeneLMNA
is asnp
is mentioned by
dbSNPrs797044486
ebirs797044486
HLIrs797044486
Exacrs797044486
Varsomers797044486
Maprs797044486
PheGenIrs797044486
hapmaprs797044486
1000 genomesrs797044486
hgdprs797044486
ensemblrs797044486
gopubmedrs797044486
geneviewrs797044486
scholarrs797044486
googlers797044486
pharmgkbrs797044486
gwascentralrs797044486
openSNPrs797044486
23andMers797044486
23andMe allrs797044486
SNP Nexus

SNPshotrs797044486
SNPdbers797044486
MSV3drs797044486
GWAS Ctlgrs797044486
Max Magnitude0
ClinVar
Risk rs797044486(A;A)
Alt rs797044486(A;A)
Reference rs797044486(T;T)
Significance Pathogenic
Disease Hutchinson-Gilford syndrome
Variation info
Gene LMNA
CLNDBN Hutchinson-Gilford syndrome
Reversed 0
HGVS NC_000001.10:g.156108351T>A
CLNSRC
CLNACC RCV000192014.1,