rs59886214

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs59886214(A;A)

Make rs59886214(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

156138610

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs59886214
dbSNP (classic)	rs59886214
ClinGen	rs59886214
ebi	rs59886214
HLI	rs59886214
Exac	rs59886214
Gnomad	rs59886214
Varsome	rs59886214
LitVar	rs59886214
Map	rs59886214
PheGenI	rs59886214
Biobank	rs59886214
1000 genomes	rs59886214
hgdp	rs59886214
ensembl	rs59886214
geneview	rs59886214
scholar	rs59886214
google	rs59886214
pharmgkb	rs59886214
gwascentral	rs59886214
openSNP	rs59886214
23andMe	rs59886214
SNPshot	rs59886214
SNPdbe	rs59886214
MSV3d	rs59886214
GWAS Ctlg	rs59886214

Max Magnitude

0

OMIM	150330
Desc
Variant	0040
Related	also

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,