rs515726196

Orientation

plus

Stabilized

plus

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

Make rs515726196(A;C)

Make rs515726196(C;C)

Reference

GRCh38 38.1/142

Chromosome

8

Position

102218827

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs515726196
dbSNP (classic)	rs515726196
ClinGen	rs515726196
ebi	rs515726196
HLI	rs515726196
Exac	rs515726196
Gnomad	rs515726196
Varsome	rs515726196
LitVar	rs515726196
Map	rs515726196
PheGenI	rs515726196
Biobank	rs515726196
1000 genomes	rs515726196
hgdp	rs515726196
ensembl	rs515726196
geneview	rs515726196
scholar	rs515726196
google	rs515726196
pharmgkb	rs515726196
gwascentral	rs515726196
openSNP	rs515726196
23andMe	rs515726196
SNPshot	rs515726196
SNPdbe	rs515726196
MSV3d	rs515726196
GWAS Ctlg	rs515726196

Max Magnitude

0

ClinVar
Risk	rs515726196(C;C)
Alt	rs515726196(C;C)
Reference	Rs515726196(A;A)
Significance	Pathogenic
Disease	RRM2B-related mitochondrial disease not provided
Variation	info
Gene	RRM2B
CLNDBN	RRM2B-related mitochondrial disease not provided
Reversed	0
HGVS	NC_000008.10:g.103231055A>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000119006.2, RCV000199478.2,