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rs794728600

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728600(C;C)
Make rs794728600(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156114995
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728600
ebirs794728600
HLIrs794728600
Exacrs794728600
Varsomers794728600
Maprs794728600
PheGenIrs794728600
hapmaprs794728600
1000 genomesrs794728600
hgdprs794728600
ensemblrs794728600
gopubmedrs794728600
geneviewrs794728600
scholarrs794728600
googlers794728600
pharmgkbrs794728600
gwascentralrs794728600
openSNPrs794728600
23andMers794728600
23andMe allrs794728600
SNP Nexus

SNPshotrs794728600
SNPdbers794728600
MSV3drs794728600
GWAS Ctlgrs794728600
Max Magnitude0
ClinVar
Risk rs794728600(C;C)
Alt rs794728600(C;C)
Reference rs794728600(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene LMNA
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.156084786T>C
CLNSRC
CLNACC RCV000182380.2,