rs515726183

Orientation

plus

Stabilized

plus

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

Make rs515726183(C;T)

Make rs515726183(T;T)

Reference

GRCh38 38.1/142

Chromosome

8

Position

102226031

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs515726183
dbSNP (classic)	rs515726183
ClinGen	rs515726183
ebi	rs515726183
HLI	rs515726183
Exac	rs515726183
Gnomad	rs515726183
Varsome	rs515726183
LitVar	rs515726183
Map	rs515726183
PheGenI	rs515726183
Biobank	rs515726183
1000 genomes	rs515726183
hgdp	rs515726183
ensembl	rs515726183
geneview	rs515726183
scholar	rs515726183
google	rs515726183
pharmgkb	rs515726183
gwascentral	rs515726183
openSNP	rs515726183
23andMe	rs515726183
SNPshot	rs515726183
SNPdbe	rs515726183
MSV3d	rs515726183
GWAS Ctlg	rs515726183

Max Magnitude

0

ClinVar
Risk	rs515726183(A;A) rs515726183(T;T)
Alt	rs515726183(A;A) rs515726183(T;T)
Reference	Rs515726183(C;C)
Significance	Pathogenic
Disease	not provided RRM2B-related mitochondrial disease
Variation	info
Gene	RRM2B
CLNDBN	not provided RRM2B-related mitochondrial disease
Reversed	0
HGVS	NC_000008.10:g.103238259C>A; NC_000008.10:g.103238259C>T
CLNSRC	ClinVar
CLNACC	RCV000196901.2, RCV000118987.2,