rs267607555

Orientation

plus

Stabilized

plus

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

Make rs267607555(C;T)

Make rs267607555(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

156136009

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs267607555
dbSNP (classic)	rs267607555
ClinGen	rs267607555
ebi	rs267607555
HLI	rs267607555
Exac	rs267607555
Gnomad	rs267607555
Varsome	rs267607555
LitVar	rs267607555
Map	rs267607555
PheGenI	rs267607555
Biobank	rs267607555
1000 genomes	rs267607555
hgdp	rs267607555
ensembl	rs267607555
geneview	rs267607555
scholar	rs267607555
google	rs267607555
pharmgkb	rs267607555
gwascentral	rs267607555
openSNP	rs267607555
23andMe	rs267607555
SNPshot	rs267607555
SNPdbe	rs267607555
MSV3d	rs267607555
GWAS Ctlg	rs267607555

Max Magnitude

0

ClinVar
Risk	rs267607555(T;T)
Alt	rs267607555(T;T)
Reference	Rs267607555(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LMNA
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.156105800C>T
CLNSRC
CLNACC	RCV000057218.2,