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rs80356807

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80356807(A;C)
Make rs80356807(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156134795
GeneLMNA
is asnp
is mentioned by
dbSNPrs80356807
ebirs80356807
HLIrs80356807
Exacrs80356807
Varsomers80356807
Maprs80356807
PheGenIrs80356807
hapmaprs80356807
1000 genomesrs80356807
hgdprs80356807
ensemblrs80356807
gopubmedrs80356807
geneviewrs80356807
scholarrs80356807
googlers80356807
pharmgkbrs80356807
gwascentralrs80356807
openSNPrs80356807
23andMers80356807
23andMe allrs80356807
SNP Nexus

SNPshotrs80356807
SNPdbers80356807
MSV3drs80356807
GWAS Ctlgrs80356807
Max Magnitude0
ClinVar
Risk rs80356807(C,G;C,G)
Alt rs80356807(C,G;C,G)
Reference rs80356807(A;A)
Significance Other
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156104586A>C; NC_000001.10:g.156104586A>G
CLNSRC
CLNACC RCV000057436.1, RCV000057437.3,