rs756933588

Orientation

plus

Stabilized

plus

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

Make rs756933588(C;T)

Make rs756933588(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

18

Position

2929065

Gene

LPIN2

is a	snp
is	mentioned by
dbSNP	rs756933588
dbSNP (classic)	rs756933588
ClinGen	rs756933588
ebi	rs756933588
HLI	rs756933588
Exac	rs756933588
Gnomad	rs756933588
Varsome	rs756933588
LitVar	rs756933588
Map	rs756933588
PheGenI	rs756933588
Biobank	rs756933588
1000 genomes	rs756933588
hgdp	rs756933588
ensembl	rs756933588
geneview	rs756933588
scholar	rs756933588
google	rs756933588
pharmgkb	rs756933588
gwascentral	rs756933588
openSNP	rs756933588
23andMe	rs756933588
SNPshot	rs756933588
SNPdbe	rs756933588
MSV3d	rs756933588
GWAS Ctlg	rs756933588

Max Magnitude

0

ClinVar
Risk	rs756933588(T;T)
Alt	rs756933588(T;T)
Reference	Rs756933588(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LPIN2
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.2929063C>T
CLNSRC
CLNACC	RCV000217293.1,