rs61672878

Orientation

plus

Stabilized

plus

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

Make rs61672878(A;A)

Make rs61672878(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

156136094

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs61672878
dbSNP (classic)	rs61672878
ClinGen	rs61672878
ebi	rs61672878
HLI	rs61672878
Exac	rs61672878
Gnomad	rs61672878
Varsome	rs61672878
LitVar	rs61672878
Map	rs61672878
PheGenI	rs61672878
Biobank	rs61672878
1000 genomes	rs61672878
hgdp	rs61672878
ensembl	rs61672878
geneview	rs61672878
scholar	rs61672878
google	rs61672878
pharmgkb	rs61672878
gwascentral	rs61672878
openSNP	rs61672878
23andMe	rs61672878
SNPshot	rs61672878
SNPdbe	rs61672878
MSV3d	rs61672878
GWAS Ctlg	rs61672878

Max Magnitude

0

OMIM	150330
Desc
Variant	0017
Related	also

ClinVar
Risk	rs61672878(A;A) rs61672878(T;T)
Alt	rs61672878(A;A) rs61672878(T;T)
Reference	Rs61672878(G;G)
Significance	Pathogenic
Disease	Limb-girdle muscular dystrophy Dilated cardiomyopathy 1A not provided not specified
Variation	info
Gene	LMNA
CLNDBN	Limb-girdle muscular dystrophy, type 1B Dilated cardiomyopathy 1A not provided not specified
Reversed	0
HGVS	NC_000001.10:g.156105885G>A; NC_000001.10:g.156105885G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015586.26, RCV000015587.22, RCV000057235.1, RCV000057236.1, RCV000216517.1,