rs121912494

Orientation

plus

Stabilized

plus

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

Make rs121912494(A;A)

Make rs121912494(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

156137209

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs121912494
dbSNP (classic)	rs121912494
ClinGen	rs121912494
ebi	rs121912494
HLI	rs121912494
Exac	rs121912494
Gnomad	rs121912494
Varsome	rs121912494
LitVar	rs121912494
Map	rs121912494
PheGenI	rs121912494
Biobank	rs121912494
1000 genomes	rs121912494
hgdp	rs121912494
ensembl	rs121912494
geneview	rs121912494
scholar	rs121912494
google	rs121912494
pharmgkb	rs121912494
gwascentral	rs121912494
openSNP	rs121912494
23andMe	rs121912494
SNPshot	rs121912494
SNPdbe	rs121912494
MSV3d	rs121912494
GWAS Ctlg	rs121912494

Max Magnitude

0

OMIM	150330
Desc
Variant	0046
Related	also

ClinVar
Risk	rs121912494(A;A)
Alt	rs121912494(A;A)
Reference	Rs121912494(G;G)
Significance	Pathogenic
Disease	Mandibuloacral dysostosis not provided
Variation	info
Gene	LMNA
CLNDBN	Mandibuloacral dysostosis not provided
Reversed	0
HGVS	NC_000001.10:g.156107000G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015619.26, RCV000057331.1,