rs776184830

Orientation

plus

Stabilized

plus

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

Make rs776184830(A;A)

Make rs776184830(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

102232235

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs776184830
dbSNP (classic)	rs776184830
ClinGen	rs776184830
ebi	rs776184830
HLI	rs776184830
Exac	rs776184830
Gnomad	rs776184830
Varsome	rs776184830
LitVar	rs776184830
Map	rs776184830
PheGenI	rs776184830
Biobank	rs776184830
1000 genomes	rs776184830
hgdp	rs776184830
ensembl	rs776184830
geneview	rs776184830
scholar	rs776184830
google	rs776184830
pharmgkb	rs776184830
gwascentral	rs776184830
openSNP	rs776184830
23andMe	rs776184830
SNPshot	rs776184830
SNPdbe	rs776184830
MSV3d	rs776184830
GWAS Ctlg	rs776184830

Max Magnitude

0

ClinVar
Risk	rs776184830(A;A)
Alt	rs776184830(A;A)
Reference	Rs776184830(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	RRM2B
CLNDBN	not provided
Reversed	0
HGVS	NC_000008.10:g.103244463G>A
CLNSRC
CLNACC	RCV000198415.2,