rs267607618

Orientation

plus

Stabilized

plus

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

Make rs267607618(C;T)

Make rs267607618(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

156136350

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs267607618
dbSNP (classic)	rs267607618
ClinGen	rs267607618
ebi	rs267607618
HLI	rs267607618
Exac	rs267607618
Gnomad	rs267607618
Varsome	rs267607618
LitVar	rs267607618
Map	rs267607618
PheGenI	rs267607618
Biobank	rs267607618
1000 genomes	rs267607618
hgdp	rs267607618
ensembl	rs267607618
geneview	rs267607618
scholar	rs267607618
google	rs267607618
pharmgkb	rs267607618
gwascentral	rs267607618
openSNP	rs267607618
23andMe	rs267607618
SNPshot	rs267607618
SNPdbe	rs267607618
MSV3d	rs267607618
GWAS Ctlg	rs267607618

Max Magnitude

0

ClinVar
Risk	rs267607618(T;T)
Alt	rs267607618(T;T)
Reference	Rs267607618(C;C)
Significance	Pathogenic
Disease	not provided Primary dilated cardiomyopathy Charcot-Marie-Tooth disease
Variation	info
Gene	LMNA
CLNDBN	not provided Primary dilated cardiomyopathy Charcot-Marie-Tooth disease, type 2
Reversed	0
HGVS	NC_000001.10:g.156106141C>T
CLNSRC
CLNACC	RCV000057263.1, RCV000216125.1, RCV000230676.2,