rs1057519172

Orientation

plus

Stabilized

plus

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

Make rs1057519172(A;A)

Make rs1057519172(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

37744354

Gene

ERLIN2

is a	snp
is	mentioned by
dbSNP	rs1057519172
dbSNP (classic)	rs1057519172
ClinGen	rs1057519172
ebi	rs1057519172
HLI	rs1057519172
Exac	rs1057519172
Gnomad	rs1057519172
Varsome	rs1057519172
LitVar	rs1057519172
Map	rs1057519172
PheGenI	rs1057519172
Biobank	rs1057519172
1000 genomes	rs1057519172
hgdp	rs1057519172
ensembl	rs1057519172
geneview	rs1057519172
scholar	rs1057519172
google	rs1057519172
pharmgkb	rs1057519172
gwascentral	rs1057519172
openSNP	rs1057519172
23andMe	rs1057519172
SNPshot	rs1057519172
SNPdbe	rs1057519172
MSV3d	rs1057519172
GWAS Ctlg	rs1057519172

Max Magnitude

0

ClinVar
Risk	rs1057519172(A;A)
Alt	rs1057519172(A;A)
Reference	Rs1057519172(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ERLIN2
CLNDBN	not provided
Reversed	0
HGVS	NC_000008.10:g.37601872G>A
CLNSRC
CLNACC	RCV000416259.1,