rs547662448

Orientation

plus

Stabilized

plus

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

Make rs547662448(A;A)

Make rs547662448(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

18

Position

2920334

Gene

LPIN2

is a	snp
is	mentioned by
dbSNP	rs547662448
dbSNP (classic)	rs547662448
ClinGen	rs547662448
ebi	rs547662448
HLI	rs547662448
Exac	rs547662448
Gnomad	rs547662448
Varsome	rs547662448
LitVar	rs547662448
Map	rs547662448
PheGenI	rs547662448
Biobank	rs547662448
1000 genomes	rs547662448
hgdp	rs547662448
ensembl	rs547662448
geneview	rs547662448
scholar	rs547662448
google	rs547662448
pharmgkb	rs547662448
gwascentral	rs547662448
openSNP	rs547662448
23andMe	rs547662448
SNPshot	rs547662448
SNPdbe	rs547662448
MSV3d	rs547662448
GWAS Ctlg	rs547662448

Max Magnitude

0

ClinVar
Risk	rs547662448(A;A)
Alt	rs547662448(A;A)
Reference	Rs547662448(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LPIN2
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.2920332G>A
CLNSRC
CLNACC	RCV000222683.1,