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rs371546359

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs371546359(A;A)
Make rs371546359(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position69419606
GeneNFU1
is asnp
is mentioned by
dbSNPrs371546359
ebirs371546359
HLIrs371546359
Exacrs371546359
Varsomers371546359
Maprs371546359
PheGenIrs371546359
hapmaprs371546359
1000 genomesrs371546359
hgdprs371546359
ensemblrs371546359
gopubmedrs371546359
geneviewrs371546359
scholarrs371546359
googlers371546359
pharmgkbrs371546359
gwascentralrs371546359
openSNPrs371546359
23andMers371546359
23andMe allrs371546359
SNP Nexus

SNPshotrs371546359
SNPdbers371546359
MSV3drs371546359
GWAS Ctlgrs371546359
Max Magnitude0
ClinVar
Risk rs371546359(A;A)
Alt rs371546359(A;A)
Reference rs371546359(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene NFU1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.69646738T>A
CLNSRC
CLNACC RCV000198803.1,