rs515726188

Orientation

plus

Stabilized

plus

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

Make rs515726188(C;T)

Make rs515726188(T;T)

Reference

GRCh38 38.1/142

Chromosome

8

Position

102224949

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs515726188
dbSNP (classic)	rs515726188
ClinGen	rs515726188
ebi	rs515726188
HLI	rs515726188
Exac	rs515726188
Gnomad	rs515726188
Varsome	rs515726188
LitVar	rs515726188
Map	rs515726188
PheGenI	rs515726188
Biobank	rs515726188
1000 genomes	rs515726188
hgdp	rs515726188
ensembl	rs515726188
geneview	rs515726188
scholar	rs515726188
google	rs515726188
pharmgkb	rs515726188
gwascentral	rs515726188
openSNP	rs515726188
23andMe	rs515726188
SNPshot	rs515726188
SNPdbe	rs515726188
MSV3d	rs515726188
GWAS Ctlg	rs515726188

Max Magnitude

0

ClinVar
Risk	rs515726188(T;T)
Alt	rs515726188(T;T)
Reference	Rs515726188(C;C)
Significance	Pathogenic
Disease	RRM2B-related mitochondrial disease
Variation	info
Gene	RRM2B
CLNDBN	RRM2B-related mitochondrial disease
Reversed	0
HGVS	NC_000008.10:g.103237177C>T
CLNSRC	ClinVar
CLNACC	RCV000118996.2,