rs80338938

Orientation

plus

Stabilized

plus

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

Make rs80338938(A;A)

Make rs80338938(A;C)

Reference

GRCh38 38.1/141

Chromosome

1

Position

156137756

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs80338938
dbSNP (classic)	rs80338938
ClinGen	rs80338938
ebi	rs80338938
HLI	rs80338938
Exac	rs80338938
Gnomad	rs80338938
Varsome	rs80338938
LitVar	rs80338938
Map	rs80338938
PheGenI	rs80338938
Biobank	rs80338938
1000 genomes	rs80338938
hgdp	rs80338938
ensembl	rs80338938
geneview	rs80338938
scholar	rs80338938
google	rs80338938
pharmgkb	rs80338938
gwascentral	rs80338938
openSNP	rs80338938
23andMe	rs80338938
SNPshot	rs80338938
SNPdbe	rs80338938
MSV3d	rs80338938
GWAS Ctlg	rs80338938

Max Magnitude

0

OMIM	150330
Desc
Variant	0009
Related	also

ClinVar
Risk	rs80338938(A;A) rs80338938(T;T)
Alt	rs80338938(A;A) rs80338938(T;T)
Reference	Rs80338938(C;C)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 1A not provided
Variation	info
Gene	LMNA
CLNDBN	Dilated cardiomyopathy 1A not provided
Reversed	0
HGVS	NC_000001.10:g.156107547C>A; NC_000001.10:g.156107547C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015574.25, RCV000057044.1, RCV000057045.1,

[PMID 10580070] Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.