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rs59886214

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs59886214(A;A)
Make rs59886214(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position156138610
GeneLMNA
is asnp
is mentioned by
dbSNPrs59886214
ebirs59886214
HLIrs59886214
Exacrs59886214
Varsomers59886214
Maprs59886214
PheGenIrs59886214
hapmaprs59886214
1000 genomesrs59886214
hgdprs59886214
ensemblrs59886214
gopubmedrs59886214
geneviewrs59886214
scholarrs59886214
googlers59886214
pharmgkbrs59886214
gwascentralrs59886214
openSNPrs59886214
23andMers59886214
23andMe allrs59886214
SNP Nexus

SNPshotrs59886214
SNPdbers59886214
MSV3drs59886214
GWAS Ctlgrs59886214
Max Magnitude0
OMIM150330
Desc
Variant0040
Relatedalso


ClinVar
Risk rs59886214(A;A)
Alt rs59886214(A;A)
Reference rs59886214(G;G)
Significance Pathogenic
Disease Hutchinson-Gilford syndrome not provided
Variation info
Gene LMNA
CLNDBN Hutchinson-Gilford syndrome not provided
Reversed 0
HGVS NC_000001.10:g.156108401G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015611.22, RCV000057362.1,