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

rs1057519727

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519727(C;C)
Make rs1057519727(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position28260829
GeneHERC2
is asnp
is mentioned by
dbSNPrs1057519727
dbSNP (old)rs1057519727
ClinGenrs1057519727
ebirs1057519727
HLIrs1057519727
Exacrs1057519727
Gnomadrs1057519727
Varsomers1057519727
LitVarrs1057519727
Maprs1057519727
PheGenIrs1057519727
Biobankrs1057519727
1000 genomesrs1057519727
hgdprs1057519727
ensemblrs1057519727
gopubmedrs1057519727
geneviewrs1057519727
scholarrs1057519727
googlers1057519727
pharmgkbrs1057519727
gwascentralrs1057519727
openSNPrs1057519727
23andMers1057519727
23andMe allrs1057519727
SNPshotrs1057519727
SNPdbers1057519727
MSV3drs1057519727
GWAS Ctlgrs1057519727
Max Magnitude0
ClinVar
Risk rs1057519727(C;C)
Alt rs1057519727(C;C)
Reference Rs1057519727(T;T)
Significance Pathogenic
Disease Neoplasm of breast
Variation info
Gene HERC2
CLNDBN Neoplasm of breast
Reversed 1
HGVS NC_000015.9:g.28505975A>G
CLNSRC
CLNACC RCV000419806.1,