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rs267607570

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607570(C;C)
Make rs267607570(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156130757
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607570
ebirs267607570
HLIrs267607570
Exacrs267607570
Varsomers267607570
Maprs267607570
PheGenIrs267607570
hapmaprs267607570
1000 genomesrs267607570
hgdprs267607570
ensemblrs267607570
gopubmedrs267607570
geneviewrs267607570
scholarrs267607570
googlers267607570
pharmgkbrs267607570
gwascentralrs267607570
openSNPrs267607570
23andMers267607570
23andMe allrs267607570
SNP Nexus

SNPshotrs267607570
SNPdbers267607570
MSV3drs267607570
GWAS Ctlgrs267607570
Max Magnitude0
ClinVar
Risk rs267607570(A,C;A,C)
Alt rs267607570(A,C;A,C)
Reference rs267607570(G;G)
Significance Pathogenic
Disease not specified not provided
Variation info
Gene LMNA
CLNDBN not specified not provided
Reversed 0
HGVS NC_000001.10:g.156100548G>A; NC_000001.10:g.156100548G>C
CLNSRC
CLNACC RCV000150939.1, RCV000057411.3,