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rs876661352

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs876661352(-;-)
Make rs876661352(-;CT)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position156135931
GeneLMNA
is asnp
is mentioned by
dbSNPrs876661352
ebirs876661352
HLIrs876661352
Exacrs876661352
Varsomers876661352
Maprs876661352
PheGenIrs876661352
hapmaprs876661352
1000 genomesrs876661352
hgdprs876661352
ensemblrs876661352
gopubmedrs876661352
geneviewrs876661352
scholarrs876661352
googlers876661352
pharmgkbrs876661352
gwascentralrs876661352
openSNPrs876661352
23andMers876661352
23andMe allrs876661352
SNP Nexus

SNPshotrs876661352
SNPdbers876661352
MSV3drs876661352
GWAS Ctlgrs876661352
Max Magnitude0
ClinVar
Risk rs876661352(;)
Alt rs876661352(;)
Reference rs876661352(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156105722_156105723delCT
CLNSRC
CLNACC RCV000223918.1,