Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728605

From SNPedia

Orientationplus
Geno Mag Summary
(GAT;GAT) 0 common in clinvar
Make rs794728605(GAT;TGGTCACCTGAGAG)
Make rs794728605(TGGTCACCTGAGAG;TGGTCACCTGAGAG)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156130641
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728605
ebirs794728605
HLIrs794728605
Exacrs794728605
Varsomers794728605
Maprs794728605
PheGenIrs794728605
hapmaprs794728605
1000 genomesrs794728605
hgdprs794728605
ensemblrs794728605
gopubmedrs794728605
geneviewrs794728605
scholarrs794728605
googlers794728605
pharmgkbrs794728605
gwascentralrs794728605
openSNPrs794728605
23andMers794728605
23andMe allrs794728605
SNP Nexus

SNPshotrs794728605
SNPdbers794728605
MSV3drs794728605
GWAS Ctlgrs794728605
Max Magnitude0
ClinVar
Risk rs794728605(TGGTCACCTGAGAG;TGGTCACCTGAGAG)
Alt rs794728605(TGGTCACCTGAGAG;TGGTCACCTGAGAG)
Reference Rs794728605(GAT;GAT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156100432_156100434delGATinsTGGTCACCTGAGAG
CLNSRC
CLNACC RCV000182386.2,