rs267607587

Orientation

plus

Stabilized

plus

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

Make rs267607587(C;T)

Make rs267607587(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

156134901

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs267607587
dbSNP (classic)	rs267607587
ClinGen	rs267607587
ebi	rs267607587
HLI	rs267607587
Exac	rs267607587
Gnomad	rs267607587
Varsome	rs267607587
LitVar	rs267607587
Map	rs267607587
PheGenI	rs267607587
Biobank	rs267607587
1000 genomes	rs267607587
hgdp	rs267607587
ensembl	rs267607587
geneview	rs267607587
scholar	rs267607587
google	rs267607587
pharmgkb	rs267607587
gwascentral	rs267607587
openSNP	rs267607587
23andMe	rs267607587
SNPshot	rs267607587
SNPdbe	rs267607587
MSV3d	rs267607587
GWAS Ctlg	rs267607587

Max Magnitude

0

ClinVar
Risk	rs267607587(T;T)
Alt	rs267607587(T;T)
Reference	Rs267607587(C;C)
Significance	Other
Disease	not provided
Variation	info
Gene	LMNA
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.156104692C>T
CLNSRC
CLNACC	RCV000057448.3,