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rs16958477

From SNPedia

Orientationplus
Stabilizedplus
Make rs16958477(A;A)
Make rs16958477(A;C)
Make rs16958477(C;C)
ReferenceGRCh38 38.1/141
Chromosome15
Position73926125
GeneRNASEH2B
is asnp
is mentioned by
dbSNPrs16958477
ebirs16958477
HLIrs16958477
Exacrs16958477
Varsomers16958477
Maprs16958477
PheGenIrs16958477
hapmaprs16958477
1000 genomesrs16958477
hgdprs16958477
ensemblrs16958477
gopubmedrs16958477
geneviewrs16958477
scholarrs16958477
googlers16958477
pharmgkbrs16958477
gwascentralrs16958477
openSNPrs16958477
23andMers16958477
23andMe allrs16958477
SNP Nexus

SNPshotrs16958477
SNPdbers16958477
MSV3drs16958477
GWAS Ctlgrs16958477
GMAF0.2608
Max Magnitude
? (A;A) (A;C) (C;C) 28
[PMID 21212179OA-icon.png] LOXL1 promoter haplotypes are associated with exfoliation syndrome in a US Caucasian population


[PMID 20431720OA-icon.png] Major LOXL1 risk allele is reversed in exfoliation glaucoma in a black South African population.


[PMID 26319397OA-icon.png] LOXL1 gene variants and their association with pseudoexfoliation glaucoma (XFG) in Spanish patients