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rs59601651

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs59601651(C;T)
Make rs59601651(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156138537
GeneLMNA
is asnp
is mentioned by
dbSNPrs59601651
ebirs59601651
HLIrs59601651
Exacrs59601651
Varsomers59601651
Maprs59601651
PheGenIrs59601651
hapmaprs59601651
1000 genomesrs59601651
hgdprs59601651
ensemblrs59601651
gopubmedrs59601651
geneviewrs59601651
scholarrs59601651
googlers59601651
pharmgkbrs59601651
gwascentralrs59601651
openSNPrs59601651
23andMers59601651
23andMe allrs59601651
SNP Nexus

SNPshotrs59601651
SNPdbers59601651
MSV3drs59601651
GWAS Ctlgrs59601651
Max Magnitude0
ClinVar
Risk rs59601651(G,T;G,T)
Alt rs59601651(G,T;G,T)
Reference rs59601651(C;C)
Significance Untested
Disease not specified not provided
Variation info
Gene LMNA
CLNDBN not specified not provided
Reversed 0
HGVS NC_000001.10:g.156108328C>G; NC_000001.10:g.156108328C>T
CLNSRC
CLNACC RCV000155709.1, RCV000057354.3, RCV000235168.1,