rs267607590

Orientation

plus

Stabilized

plus

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

Make rs267607590(A;A)

Make rs267607590(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

156136122

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs267607590
dbSNP (classic)	rs267607590
ClinGen	rs267607590
ebi	rs267607590
HLI	rs267607590
Exac	rs267607590
Gnomad	rs267607590
Varsome	rs267607590
LitVar	rs267607590
Map	rs267607590
PheGenI	rs267607590
Biobank	rs267607590
1000 genomes	rs267607590
hgdp	rs267607590
ensembl	rs267607590
geneview	rs267607590
scholar	rs267607590
google	rs267607590
pharmgkb	rs267607590
gwascentral	rs267607590
openSNP	rs267607590
23andMe	rs267607590
SNPshot	rs267607590
SNPdbe	rs267607590
MSV3d	rs267607590
GWAS Ctlg	rs267607590

Max Magnitude

0

ClinVar
Risk	rs267607590(A;A) rs267607590(T;T)
Alt	rs267607590(A;A) rs267607590(T;T)
Reference	Rs267607590(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LMNA
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.156105913G>A; NC_000001.10:g.156105913G>T
CLNSRC
CLNACC	RCV000057242.3, RCV000236305.1,