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rs730881615

From SNPedia

Orientationplus
Geno Mag Summary
(GGTATGCTGTTA;GGTATGCTGTTA) 0 common in clinvar
Make rs730881615(GGTATGCTGTTA;TT)
Make rs730881615(TT;TT)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32363376
GeneBRCA2
is asnp
is mentioned by
dbSNPrs730881615
ebirs730881615
HLIrs730881615
Exacrs730881615
Varsomers730881615
Maprs730881615
PheGenIrs730881615
hapmaprs730881615
1000 genomesrs730881615
hgdprs730881615
ensemblrs730881615
gopubmedrs730881615
geneviewrs730881615
scholarrs730881615
googlers730881615
pharmgkbrs730881615
gwascentralrs730881615
openSNPrs730881615
23andMers730881615
23andMe allrs730881615
SNP Nexus

SNPshotrs730881615
SNPdbers730881615
MSV3drs730881615
GWAS Ctlgrs730881615
Max Magnitude0
ClinVar
Risk rs730881615(TT;TT)
Alt rs730881615(TT;TT)
Reference rs730881615(GGTATGCTGTTA;GGTATGCTGTTA)
Significance Pathogenic
Disease not provided
Variation info
Gene BRCA2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32937513_32937524delGGTATGCTGTTAinsTT
CLNSRC
CLNACC RCV000160307.2,