rs752097874

Orientation

plus

Stabilized

plus

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

Make rs752097874(C;C)

Make rs752097874(C;G)

Reference

GRCh38.p7 38.3/149

Chromosome

15

Position

23645747

Gene

MAGEL2

is a	snp
is	mentioned by
dbSNP	rs752097874
dbSNP (classic)	rs752097874
ClinGen	rs752097874
ebi	rs752097874
HLI	rs752097874
Exac	rs752097874
Gnomad	rs752097874
Varsome	rs752097874
LitVar	rs752097874
Map	rs752097874
PheGenI	rs752097874
Biobank	rs752097874
1000 genomes	rs752097874
hgdp	rs752097874
ensembl	rs752097874
geneview	rs752097874
scholar	rs752097874
google	rs752097874
pharmgkb	rs752097874
gwascentral	rs752097874
openSNP	rs752097874
23andMe	rs752097874
SNPshot	rs752097874
SNPdbe	rs752097874
MSV3d	rs752097874
GWAS Ctlg	rs752097874

Max Magnitude

0

ClinVar
Risk	rs752097874(A;A) rs752097874(C;C) rs752097874(T;T)
Alt	rs752097874(A;A) rs752097874(C;C) rs752097874(T;T)
Reference	Rs752097874(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MAGEL2
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.23890894G>A
CLNSRC
CLNACC	RCV000254810.1,