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rs368386019

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs368386019(A;A)
Make rs368386019(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156138720
GeneLMNA
is asnp
is mentioned by
dbSNPrs368386019
ebirs368386019
HLIrs368386019
Exacrs368386019
Varsomers368386019
Maprs368386019
PheGenIrs368386019
hapmaprs368386019
1000 genomesrs368386019
hgdprs368386019
ensemblrs368386019
gopubmedrs368386019
geneviewrs368386019
scholarrs368386019
googlers368386019
pharmgkbrs368386019
gwascentralrs368386019
openSNPrs368386019
23andMers368386019
23andMe allrs368386019
SNP Nexus

SNPshotrs368386019
SNPdbers368386019
MSV3drs368386019
GWAS Ctlgrs368386019
Max Magnitude0
ClinVar
Risk rs368386019(A;A)
Alt rs368386019(A;A)
Reference rs368386019(G;G)
Significance Probable-non-pathogenic
Disease Congenital muscular dystrophy not specified Charcot-Marie-Tooth disease
Variation info
Gene LMNA
CLNDBN Congenital muscular dystrophy not specified Charcot-Marie-Tooth disease, type 2
Reversed 0
HGVS NC_000001.10:g.156108511G>A
CLNSRC
CLNACC RCV000148599.1, RCV000182377.2, RCV000231962.1,