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rs776184830

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs776184830(A;A)
Make rs776184830(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position102232235
GeneRRM2B
is asnp
is mentioned by
dbSNPrs776184830
ebirs776184830
HLIrs776184830
Exacrs776184830
Varsomers776184830
Maprs776184830
PheGenIrs776184830
hapmaprs776184830
1000 genomesrs776184830
hgdprs776184830
ensemblrs776184830
gopubmedrs776184830
geneviewrs776184830
scholarrs776184830
googlers776184830
pharmgkbrs776184830
gwascentralrs776184830
openSNPrs776184830
23andMers776184830
23andMe allrs776184830
SNP Nexus

SNPshotrs776184830
SNPdbers776184830
MSV3drs776184830
GWAS Ctlgrs776184830
Max Magnitude0
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,