rs121912495

Orientation

plus

Stabilized

plus

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

Make rs121912495(C;C)

Make rs121912495(C;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

156136103

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs121912495
dbSNP (classic)	rs121912495
ClinGen	rs121912495
ebi	rs121912495
HLI	rs121912495
Exac	rs121912495
Gnomad	rs121912495
Varsome	rs121912495
LitVar	rs121912495
Map	rs121912495
PheGenI	rs121912495
Biobank	rs121912495
1000 genomes	rs121912495
hgdp	rs121912495
ensembl	rs121912495
geneview	rs121912495
scholar	rs121912495
google	rs121912495
pharmgkb	rs121912495
gwascentral	rs121912495
openSNP	rs121912495
23andMe	rs121912495
SNPshot	rs121912495
SNPdbe	rs121912495
MSV3d	rs121912495
GWAS Ctlg	rs121912495

Max Magnitude

0

OMIM	150330
Desc
Variant	0047
Related	also

ClinVar
Risk	rs121912495(C;C)
Alt	rs121912495(C;C)
Reference	Rs121912495(T;T)
Significance	Pathogenic
Disease	Congenital muscular dystrophy not provided
Variation	info
Gene	LMNA
CLNDBN	Congenital muscular dystrophy, LMNA-related not provided
Reversed	0
HGVS	NC_000001.10:g.156105894T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015620.25, RCV000057237.1,