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rs757041809

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757041809(A;A)
Make rs757041809(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156134812
GeneLMNA
is asnp
is mentioned by
dbSNPrs757041809
ebirs757041809
HLIrs757041809
Exacrs757041809
Varsomers757041809
Maprs757041809
PheGenIrs757041809
hapmaprs757041809
1000 genomesrs757041809
hgdprs757041809
ensemblrs757041809
gopubmedrs757041809
geneviewrs757041809
scholarrs757041809
googlers757041809
pharmgkbrs757041809
gwascentralrs757041809
openSNPrs757041809
23andMers757041809
23andMe allrs757041809
SNP Nexus

SNPshotrs757041809
SNPdbers757041809
MSV3drs757041809
GWAS Ctlgrs757041809
Max Magnitude0
ClinVar
Risk rs757041809(A;A)
Alt rs757041809(A;A)
Reference rs757041809(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156104603G>A
CLNSRC
CLNACC RCV000182395.2,