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rs556237236

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs556237236(A;A)
Make rs556237236(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156115247
GeneLMNA
is asnp
is mentioned by
dbSNPrs556237236
ebirs556237236
HLIrs556237236
Exacrs556237236
Varsomers556237236
Maprs556237236
PheGenIrs556237236
hapmaprs556237236
1000 genomesrs556237236
hgdprs556237236
ensemblrs556237236
gopubmedrs556237236
geneviewrs556237236
scholarrs556237236
googlers556237236
pharmgkbrs556237236
gwascentralrs556237236
openSNPrs556237236
23andMers556237236
23andMe allrs556237236
SNP Nexus

SNPshotrs556237236
SNPdbers556237236
MSV3drs556237236
GWAS Ctlgrs556237236
Max Magnitude0
ClinVar
Risk rs556237236(A,C;A,C)
Alt rs556237236(A,C;A,C)
Reference rs556237236(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156085038G>C
CLNSRC
CLNACC RCV000182352.2,