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rs12946397

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs12946397(C;T)
Make rs12946397(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position58692618
GeneRAD51C, TEX14
is asnp
is mentioned by
dbSNPrs12946397
dbSNP (classic)rs12946397
ClinGenrs12946397
ebirs12946397
HLIrs12946397
Exacrs12946397
Gnomadrs12946397
Varsomers12946397
LitVarrs12946397
Maprs12946397
PheGenIrs12946397
Biobankrs12946397
1000 genomesrs12946397
hgdprs12946397
ensemblrs12946397
geneviewrs12946397
scholarrs12946397
googlers12946397
pharmgkbrs12946397
gwascentralrs12946397
openSNPrs12946397
23andMers12946397
SNPshotrs12946397
SNPdbers12946397
MSV3drs12946397
GWAS Ctlgrs12946397
Max Magnitude0

[PMID 24631219] Rad51C: a novel suppressor gene modulates the risk of head and neck cancer

[PMID 25343521OA-icon.png] Single nucleotide polymorphisms in noncoding regions of Rad51C do not change the risk of unselected breast cancer but they modulate the level of oxidative stress and the DNA damage characteristics: a case-control study

[PMID 26406419] RAD51C mutation screening in high-risk patients from Serbian hereditary breast/ovarian cancer families


ClinVar
Risk rs12946397(T;T)
Alt rs12946397(T;T)
Reference Rs12946397(C;C)
Significance Probable-non-pathogenic
Disease Breast and Ovarian Cancer Susceptibility Fanconi anemia
Variation info
Gene TEX14 RAD51C
CLNDBN Breast and Ovarian Cancer Susceptibility Fanconi anemia
Reversed 0
HGVS NC_000017.10:g.56769979C>T
CLNSRC
CLNACC RCV000269140.1, RCV000381874.1,