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rs786205448

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205448(A;A)
Make rs786205448(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156138563
GeneLMNA
is asnp
is mentioned by
dbSNPrs786205448
ebirs786205448
HLIrs786205448
Exacrs786205448
Varsomers786205448
Maprs786205448
PheGenIrs786205448
hapmaprs786205448
1000 genomesrs786205448
hgdprs786205448
ensemblrs786205448
gopubmedrs786205448
geneviewrs786205448
scholarrs786205448
googlers786205448
pharmgkbrs786205448
gwascentralrs786205448
openSNPrs786205448
23andMers786205448
23andMe allrs786205448
SNP Nexus

SNPshotrs786205448
SNPdbers786205448
MSV3drs786205448
GWAS Ctlgrs786205448
Max Magnitude0
ClinVar
Risk rs786205448(A;A)
Alt rs786205448(A;A)
Reference rs786205448(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156108354G>A
CLNSRC
CLNACC RCV000171159.1, RCV000201245.1,