rs515726189

Orientation

plus

Stabilized

plus

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

Make rs515726189(A;A)

Make rs515726189(A;G)

Reference

GRCh38 38.1/142

Chromosome

8

Position

102224909

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs515726189
dbSNP (classic)	rs515726189
ClinGen	rs515726189
ebi	rs515726189
HLI	rs515726189
Exac	rs515726189
Gnomad	rs515726189
Varsome	rs515726189
LitVar	rs515726189
Map	rs515726189
PheGenI	rs515726189
Biobank	rs515726189
1000 genomes	rs515726189
hgdp	rs515726189
ensembl	rs515726189
geneview	rs515726189
scholar	rs515726189
google	rs515726189
pharmgkb	rs515726189
gwascentral	rs515726189
openSNP	rs515726189
23andMe	rs515726189
SNPshot	rs515726189
SNPdbe	rs515726189
MSV3d	rs515726189
GWAS Ctlg	rs515726189

Max Magnitude

0

ClinVar
Risk	rs515726189(A;A)
Alt	rs515726189(A;A)
Reference	Rs515726189(G;G)
Significance	Pathogenic
Disease	RRM2B-related mitochondrial disease
Variation	info
Gene	RRM2B
CLNDBN	RRM2B-related mitochondrial disease
Reversed	0
HGVS	NC_000008.10:g.103237137G>A
CLNSRC	ClinVar
CLNACC	RCV000118997.2,