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rs2228171

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2228171(A;A)
Make rs2228171(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position169196995
GeneLRP2
is asnp
is mentioned by
dbSNPrs2228171
ebirs2228171
HLIrs2228171
Exacrs2228171
Varsomers2228171
Maprs2228171
PheGenIrs2228171
hapmaprs2228171
1000 genomesrs2228171
hgdprs2228171
ensemblrs2228171
gopubmedrs2228171
geneviewrs2228171
scholarrs2228171
googlers2228171
pharmgkbrs2228171
gwascentralrs2228171
openSNPrs2228171
23andMers2228171
23andMe allrs2228171
SNP Nexus

SNPshotrs2228171
SNPdbers2228171
MSV3drs2228171
GWAS Ctlgrs2228171
Merged fromRs4668123
GMAF0.3232
Max Magnitude0

[PMID 23274376] Cisplatin-induced ototoxicity in pediatric solid tumors: the role of glutathione S-transferases and megalin genetic polymorphisms [PMID 17457342] Megalin genetic polymorphisms and individual sensitivity to the ototoxic effect of cisplatin.


[PMID 18559602OA-icon.png] Association of megalin genetic polymorphisms with prostate cancer risk and prognosis.


[PMID 22170372OA-icon.png] Vitamin D receptor and megalin gene polymorphisms and their associations with longitudinal cognitive change in US adults.

ClinVar
Risk rs2228171(A;A)
Alt rs2228171(A;A)
Reference Rs2228171(G;G)
Significance Other
Disease not specified
Variation info
Gene LRP2
CLNDBN not specified
Reversed 1
HGVS NC_000002.11:g.170053505C>T
CLNSRC UniProtKB (protein)
CLNACC RCV000117550.3,