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rs59914820

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs59914820(C;T)
Make rs59914820(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position156115000
GeneLMNA
is asnp
is mentioned by
dbSNPrs59914820
ebirs59914820
HLIrs59914820
Exacrs59914820
Varsomers59914820
Maprs59914820
PheGenIrs59914820
hapmaprs59914820
1000 genomesrs59914820
hgdprs59914820
ensemblrs59914820
gopubmedrs59914820
geneviewrs59914820
scholarrs59914820
googlers59914820
pharmgkbrs59914820
gwascentralrs59914820
openSNPrs59914820
23andMers59914820
23andMe allrs59914820
SNP Nexus

SNPshotrs59914820
SNPdbers59914820
MSV3drs59914820
GWAS Ctlgrs59914820
Max Magnitude0
ClinVar
Risk rs59914820(G,T;G,T)
Alt rs59914820(G,T;G,T)
Reference rs59914820(C;C)
Significance Probable-Pathogenic
Disease Inborn genetic diseases not provided
Variation info
Gene LMNA
CLNDBN Inborn genetic diseases not provided
Reversed 0
HGVS NC_000001.10:g.156084791C>G; NC_000001.10:g.156084791C>T
CLNSRC
CLNACC RCV000210645.1, RCV000057473.1,