rs61661343

Orientation

plus

Stabilized

plus

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

Make rs61661343(C;C)

Make rs61661343(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

156130687

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs61661343
dbSNP (classic)	rs61661343
ClinGen	rs61661343
ebi	rs61661343
HLI	rs61661343
Exac	rs61661343
Gnomad	rs61661343
Varsome	rs61661343
LitVar	rs61661343
Map	rs61661343
PheGenI	rs61661343
Biobank	rs61661343
1000 genomes	rs61661343
hgdp	rs61661343
ensembl	rs61661343
geneview	rs61661343
scholar	rs61661343
google	rs61661343
pharmgkb	rs61661343
gwascentral	rs61661343
openSNP	rs61661343
23andMe	rs61661343
SNPshot	rs61661343
SNPdbe	rs61661343
MSV3d	rs61661343
GWAS Ctlg	rs61661343

Max Magnitude

0

ClinVar
Risk	rs61661343(C;C)
Alt	rs61661343(C;C)
Reference	Rs61661343(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LMNA
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.156100478T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057404.2,