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rs193303002

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193303002(A;A)
Make rs193303002(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeMT
Position15927
is asnp
is mentioned by
dbSNPrs193303002
ebirs193303002
HLIrs193303002
Exacrs193303002
Varsomers193303002
Maprs193303002
PheGenIrs193303002
hapmaprs193303002
1000 genomesrs193303002
hgdprs193303002
ensemblrs193303002
gopubmedrs193303002
geneviewrs193303002
scholarrs193303002
googlers193303002
pharmgkbrs193303002
gwascentralrs193303002
openSNPrs193303002
23andMers193303002
23andMe allrs193303002
SNP Nexus

SNPshotrs193303002
SNPdbers193303002
MSV3drs193303002
GWAS Ctlgrs193303002
Merged fromRs527236197
Max Magnitude0
ClinVar
Risk rs193303002(A;A)
Alt rs193303002(A;A)
Reference rs193303002(G;G)
Significance Probable-Pathogenic
Disease Familial cancer of breast
Variation info
Gene
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_012920.1:m.15927G>A
CLNSRC
CLNACC RCV000133441.1,