rs515726186

Orientation

plus

Stabilized

plus

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

Make rs515726186(A;A)

Make rs515726186(A;G)

Reference

GRCh38 38.1/142

Chromosome

8

Position

102225012

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs515726186
dbSNP (classic)	rs515726186
ClinGen	rs515726186
ebi	rs515726186
HLI	rs515726186
Exac	rs515726186
Gnomad	rs515726186
Varsome	rs515726186
LitVar	rs515726186
Map	rs515726186
PheGenI	rs515726186
Biobank	rs515726186
1000 genomes	rs515726186
hgdp	rs515726186
ensembl	rs515726186
geneview	rs515726186
scholar	rs515726186
google	rs515726186
pharmgkb	rs515726186
gwascentral	rs515726186
openSNP	rs515726186
23andMe	rs515726186
SNPshot	rs515726186
SNPdbe	rs515726186
MSV3d	rs515726186
GWAS Ctlg	rs515726186

Max Magnitude

0

ClinVar
Risk	rs515726186(A;A)
Alt	rs515726186(A;A)
Reference	Rs515726186(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.103237240G>A
CLNSRC	ClinVar
CLNACC	RCV000118991.2,