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rs113860699

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs113860699(A;A)
Make rs113860699(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156138759
GeneLMNA
is asnp
is mentioned by
dbSNPrs113860699
ebirs113860699
HLIrs113860699
Exacrs113860699
Varsomers113860699
Maprs113860699
PheGenIrs113860699
hapmaprs113860699
1000 genomesrs113860699
hgdprs113860699
ensemblrs113860699
gopubmedrs113860699
geneviewrs113860699
scholarrs113860699
googlers113860699
pharmgkbrs113860699
gwascentralrs113860699
openSNPrs113860699
23andMers113860699
23andMe allrs113860699
SNP Nexus

SNPshotrs113860699
SNPdbers113860699
MSV3drs113860699
GWAS Ctlgrs113860699
Max Magnitude0
ClinVar
Risk rs113860699(A,C,G;A,C,G)
Alt rs113860699(A,C,G;A,C,G)
Reference rs113860699(T;T)
Significance Pathogenic
Disease Hutchinson-Gilford syndrome
Variation info
Gene LMNA
CLNDBN Hutchinson-Gilford syndrome
Reversed 0
HGVS NC_000001.10:g.156108550T>A; NC_000001.10:g.156108550T>C
CLNSRC
CLNACC RCV000192017.1, RCV000192018.1,