rs515726182

Orientation

plus

Stabilized

plus

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

Make rs515726182(A;G)

Make rs515726182(G;G)

Reference

GRCh38 38.1/142

Chromosome

8

Position

102232163

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs515726182
dbSNP (classic)	rs515726182
ClinGen	rs515726182
ebi	rs515726182
HLI	rs515726182
Exac	rs515726182
Gnomad	rs515726182
Varsome	rs515726182
LitVar	rs515726182
Map	rs515726182
PheGenI	rs515726182
Biobank	rs515726182
1000 genomes	rs515726182
hgdp	rs515726182
ensembl	rs515726182
geneview	rs515726182
scholar	rs515726182
google	rs515726182
pharmgkb	rs515726182
gwascentral	rs515726182
openSNP	rs515726182
23andMe	rs515726182
SNPshot	rs515726182
SNPdbe	rs515726182
MSV3d	rs515726182
GWAS Ctlg	rs515726182

Max Magnitude

0

ClinVar
Risk	rs515726182(G;G)
Alt	rs515726182(G;G)
Reference	Rs515726182(A;A)
Significance	Pathogenic
Disease	RRM2B-related mitochondrial disease
Variation	info
Gene	RRM2B
CLNDBN	RRM2B-related mitochondrial disease
Reversed	0
HGVS	NC_000008.10:g.103244391A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000118986.2,