rs61282106

Orientation

plus

Stabilized

plus

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

Make rs61282106(A;A)

Make rs61282106(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

156136934

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs61282106
dbSNP (classic)	rs61282106
ClinGen	rs61282106
ebi	rs61282106
HLI	rs61282106
Exac	rs61282106
Gnomad	rs61282106
Varsome	rs61282106
LitVar	rs61282106
Map	rs61282106
PheGenI	rs61282106
Biobank	rs61282106
1000 genomes	rs61282106
hgdp	rs61282106
ensembl	rs61282106
geneview	rs61282106
scholar	rs61282106
google	rs61282106
pharmgkb	rs61282106
gwascentral	rs61282106
openSNP	rs61282106
23andMe	rs61282106
SNPshot	rs61282106
SNPdbe	rs61282106
MSV3d	rs61282106
GWAS Ctlg	rs61282106

Max Magnitude

0

OMIM	150330
Desc
Variant	0015
Related	also

ClinVar
Risk	rs61282106(A;A)
Alt	rs61282106(A;A)
Reference	Rs61282106(G;G)
Significance	Pathogenic
Disease	Familial partial lipodystrophy 2 not provided
Variation	info
Gene	LMNA
CLNDBN	Familial partial lipodystrophy 2 not provided
Reversed	0
HGVS	NC_000001.10:g.156106725G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015584.26, RCV000057287.1,