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rs139875047

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs139875047(A;A)
Make rs139875047(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position156130699
GeneLMNA
is asnp
is mentioned by
dbSNPrs139875047
dbSNP (classic)rs139875047
ClinGenrs139875047
ebirs139875047
HLIrs139875047
Exacrs139875047
Gnomadrs139875047
Varsomers139875047
LitVarrs139875047
Maprs139875047
PheGenIrs139875047
Biobankrs139875047
1000 genomesrs139875047
hgdprs139875047
ensemblrs139875047
geneviewrs139875047
scholarrs139875047
googlers139875047
pharmgkbrs139875047
gwascentralrs139875047
openSNPrs139875047
23andMers139875047
23andMe allrs139875047
SNPshotrs139875047
SNPdbers139875047
MSV3drs139875047
GWAS Ctlgrs139875047
Max Magnitude0
ClinVar
Risk rs139875047(A;A) rs139875047(T;T)
Alt rs139875047(A;A) rs139875047(T;T)
Reference Rs139875047(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156100490G>C
CLNSRC
CLNACC RCV000493099.1,