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

rs17848169

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs17848169(A;G)
Make rs17848169(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position169204093
GeneLRP2
is asnp
is mentioned by
dbSNPrs17848169
ebirs17848169
HLIrs17848169
Exacrs17848169
Varsomers17848169
Maprs17848169
PheGenIrs17848169
hapmaprs17848169
1000 genomesrs17848169
hgdprs17848169
ensemblrs17848169
gopubmedrs17848169
geneviewrs17848169
scholarrs17848169
googlers17848169
pharmgkbrs17848169
gwascentralrs17848169
openSNPrs17848169
23andMers17848169
23andMe allrs17848169
SNP Nexus

SNPshotrs17848169
SNPdbers17848169
MSV3drs17848169
GWAS Ctlgrs17848169
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 27197912] Association Analysis of the Cubilin (CUBN) and Megalin (LRP2) Genes with ESRD in African Americans.


ClinVar
Risk rs17848169(C,G,T;C,G,T)
Alt rs17848169(C,G,T;C,G,T)
Reference rs17848169(A;A)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene LRP2
CLNDBN not specified
Reversed 1
HGVS NC_000002.11:g.170060603T>C
CLNSRC
CLNACC RCV000117548.2,