Have questions? Visit https://www.reddit.com/r/SNPedia

rs727503760

From SNPedia

Orientationplus
Geno Mag Summary
(GTAA;GTAA) 0 common in clinvar
Make rs727503760(-;-)
Make rs727503760(-;AGTA)
Make rs727503760(AGTA;AGTA)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position58709994
GeneRAD51C
is asnp
is mentioned by
dbSNPrs727503760
ebirs727503760
HLIrs727503760
Exacrs727503760
Varsomers727503760
Maprs727503760
PheGenIrs727503760
hapmaprs727503760
1000 genomesrs727503760
hgdprs727503760
ensemblrs727503760
gopubmedrs727503760
geneviewrs727503760
scholarrs727503760
googlers727503760
pharmgkbrs727503760
gwascentralrs727503760
openSNPrs727503760
23andMers727503760
23andMe allrs727503760
SNP Nexus

SNPshotrs727503760
SNPdbers727503760
MSV3drs727503760
GWAS Ctlgrs727503760
Max Magnitude0
ClinVar
Risk rs727503760(;)
Alt rs727503760(;)
Reference rs727503760(GTAA;GTAA)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene RAD51C
CLNDBN Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000017.10:g.56787355_56787358delAGTA
CLNSRC
CLNACC RCV000116181.2, RCV000218930.1,