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rs6917

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs6917(C;T)
Make rs6917(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position49404181
GenePHB
is asnp
is mentioned by
dbSNPrs6917
dbSNP (classic)rs6917
ClinGenrs6917
ebirs6917
HLIrs6917
Exacrs6917
Gnomadrs6917
Varsomers6917
LitVarrs6917
Maprs6917
PheGenIrs6917
Biobankrs6917
1000 genomesrs6917
hgdprs6917
ensemblrs6917
geneviewrs6917
scholarrs6917
googlers6917
pharmgkbrs6917
gwascentralrs6917
openSNPrs6917
23andMers6917
SNPshotrs6917
SNPdbers6917
MSV3drs6917
GWAS Ctlgrs6917
GMAF0.1814
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 22669161OA-icon.png] Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study


[PMID 23662067OA-icon.png] 3' untranslated region 1630 C>T polymorphism of prohibitin increases risk of breast cancer


[PMID 24879411OA-icon.png] Prohibitin Expression Deregulation in Gastric Cancer Is Associated with the 3' Untranslated Region 1630 C>T Polymorphism and Copy Number Variation