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rs875989821

From SNPedia

Orientationplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs875989821(-;-)
Make rs875989821(-;TG)
Make rs875989821(TG;TG)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position46702736
GeneZNF408
is asnp
is mentioned by
dbSNPrs875989821
ebirs875989821
HLIrs875989821
Exacrs875989821
Varsomers875989821
Maprs875989821
PheGenIrs875989821
hapmaprs875989821
1000 genomesrs875989821
hgdprs875989821
ensemblrs875989821
gopubmedrs875989821
geneviewrs875989821
scholarrs875989821
googlers875989821
pharmgkbrs875989821
gwascentralrs875989821
openSNPrs875989821
23andMers875989821
23andMe allrs875989821
SNP Nexus

SNPshotrs875989821
SNPdbers875989821
MSV3drs875989821
GWAS Ctlgrs875989821
Max Magnitude0
ClinVar
Risk rs875989821(;)
Alt rs875989821(;)
Reference rs875989821(GT;GT)
Significance Pathogenic
Disease Retinitis pigmentosa 72
Variation info
Gene ZNF408
CLNDBN Retinitis pigmentosa 72
Reversed 0
HGVS NC_000011.9:g.46724286_46724287delTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000186511.2,