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rs876657649

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657649(C;G)
Make rs876657649(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position156136074
GeneLMNA
is asnp
is mentioned by
dbSNPrs876657649
ebirs876657649
HLIrs876657649
Exacrs876657649
Varsomers876657649
Maprs876657649
PheGenIrs876657649
hapmaprs876657649
1000 genomesrs876657649
hgdprs876657649
ensemblrs876657649
gopubmedrs876657649
geneviewrs876657649
scholarrs876657649
googlers876657649
pharmgkbrs876657649
gwascentralrs876657649
openSNPrs876657649
23andMers876657649
23andMe allrs876657649
SNP Nexus

SNPshotrs876657649
SNPdbers876657649
MSV3drs876657649
GWAS Ctlgrs876657649
Max Magnitude0
ClinVar
Risk rs876657649(G;G)
Alt rs876657649(G;G)
Reference rs876657649(C;C)
Significance Probable-Pathogenic
Disease Laminopathy
Variation info
Gene LMNA
CLNDBN Laminopathy
Reversed 0
HGVS NC_000001.10:g.156105865C>G
CLNSRC
CLNACC RCV000223064.1,