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rs797044487

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044487(A;A)
Make rs797044487(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156138757
GeneLMNA
is asnp
is mentioned by
dbSNPrs797044487
ebirs797044487
HLIrs797044487
Exacrs797044487
Varsomers797044487
Maprs797044487
PheGenIrs797044487
hapmaprs797044487
1000 genomesrs797044487
hgdprs797044487
ensemblrs797044487
gopubmedrs797044487
geneviewrs797044487
scholarrs797044487
googlers797044487
pharmgkbrs797044487
gwascentralrs797044487
openSNPrs797044487
23andMers797044487
23andMe allrs797044487
SNP Nexus

SNPshotrs797044487
SNPdbers797044487
MSV3drs797044487
GWAS Ctlgrs797044487
Max Magnitude0
ClinVar
Risk rs797044487(A;A)
Alt rs797044487(A;A)
Reference rs797044487(G;G)
Significance Pathogenic
Disease Hutchinson-Gilford progeria syndrome Hutchinson-Gilford syndrome
Variation info
Gene LMNA
CLNDBN Hutchinson-Gilford progeria syndrome, atypical Hutchinson-Gilford syndrome
Reversed 0
HGVS NC_000001.10:g.156108548G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000190822.3, RCV000192015.1,