rs139875047

Orientation

plus

Stabilized

plus

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

Make rs139875047(A;A)

Make rs139875047(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

156130699

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs139875047
dbSNP (classic)	rs139875047
ClinGen	rs139875047
ebi	rs139875047
HLI	rs139875047
Exac	rs139875047
Gnomad	rs139875047
Varsome	rs139875047
LitVar	rs139875047
Map	rs139875047
PheGenI	rs139875047
Biobank	rs139875047
1000 genomes	rs139875047
hgdp	rs139875047
ensembl	rs139875047
geneview	rs139875047
scholar	rs139875047
google	rs139875047
pharmgkb	rs139875047
gwascentral	rs139875047
openSNP	rs139875047
23andMe	rs139875047
SNPshot	rs139875047
SNPdbe	rs139875047
MSV3d	rs139875047
GWAS Ctlg	rs139875047

Max Magnitude

0

ClinVar
Risk	rs139875047(A;A) rs139875047(T;T)
Alt	rs139875047(A;A) rs139875047(T;T)
Reference	Rs139875047(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LMNA
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.156100490G>C
CLNSRC
CLNACC	RCV000493099.1,