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

rs281865162

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTTCCCGGGAACACC;CTTCCCGGGAACACC) 0 common in clinvar
(TTCCCGGGAACACCC;TTCCCGGGAACACCC) 0 common in clinvar
Make rs281865162(-;-)
Make rs281865162(-;TTCCCGGGAACACCC)
ReferenceGRCh38 38.1/142
Chromosome16
Position88436565
GeneZNF469
is asnp
is mentioned by
dbSNPrs281865162
dbSNP (old)rs281865162
ClinGenrs281865162
ebirs281865162
HLIrs281865162
Exacrs281865162
Gnomadrs281865162
Varsomers281865162
Maprs281865162
PheGenIrs281865162
Biobankrs281865162
1000 genomesrs281865162
hgdprs281865162
ensemblrs281865162
gopubmedrs281865162
geneviewrs281865162
scholarrs281865162
googlers281865162
pharmgkbrs281865162
gwascentralrs281865162
openSNPrs281865162
23andMers281865162
23andMe allrs281865162
SNP Nexus

SNPshotrs281865162
SNPdbers281865162
MSV3drs281865162
GWAS Ctlgrs281865162
Max Magnitude0
ClinVar
Risk rs281865162(-;-) Rs281865162(CTTCCCGGGAACACC;CTTCCCGGGAACACC)
Alt rs281865162(-;-) Rs281865162(CTTCCCGGGAACACC;CTTCCCGGGAACACC)
Reference Rs281865162(TTCCCGGGAACACCC;TTCCCGGGAACACCC)
Significance Pathogenic
Disease Keratoconus 1 not specified
Variation info
Gene ZNF469
CLNDBN Keratoconus 1 not specified
Reversed 0
HGVS NC_000016.9:g.88502973_88502987delTTCCCGGGAACACCC
CLNSRC ClinVar
CLNACC RCV000114803.1, RCV000480968.1,