rs515726181

Orientation

plus

Stabilized

plus

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

Make rs515726181(A;A)

Make rs515726181(A;G)

Reference

GRCh38 38.1/142

Chromosome

8

Position

102232232

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs515726181
dbSNP (classic)	rs515726181
ClinGen	rs515726181
ebi	rs515726181
HLI	rs515726181
Exac	rs515726181
Gnomad	rs515726181
Varsome	rs515726181
LitVar	rs515726181
Map	rs515726181
PheGenI	rs515726181
Biobank	rs515726181
1000 genomes	rs515726181
hgdp	rs515726181
ensembl	rs515726181
geneview	rs515726181
scholar	rs515726181
google	rs515726181
pharmgkb	rs515726181
gwascentral	rs515726181
openSNP	rs515726181
23andMe	rs515726181
SNPshot	rs515726181
SNPdbe	rs515726181
MSV3d	rs515726181
GWAS Ctlg	rs515726181

Max Magnitude

0

ClinVar
Risk	rs515726181(A;A)
Alt	rs515726181(A;A)
Reference	Rs515726181(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.103244460G>A
CLNSRC	ClinVar
CLNACC	RCV000118983.2,