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rs875989805

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs875989805(C;T)
Make rs875989805(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position17687870
GeneNHS
is asnp
is mentioned by
dbSNPrs875989805
ebirs875989805
HLIrs875989805
Exacrs875989805
Varsomers875989805
Maprs875989805
PheGenIrs875989805
hapmaprs875989805
1000 genomesrs875989805
hgdprs875989805
ensemblrs875989805
gopubmedrs875989805
geneviewrs875989805
scholarrs875989805
googlers875989805
pharmgkbrs875989805
gwascentralrs875989805
openSNPrs875989805
23andMers875989805
23andMe allrs875989805
SNP Nexus

SNPshotrs875989805
SNPdbers875989805
MSV3drs875989805
GWAS Ctlgrs875989805
Max Magnitude0
ClinVar
Risk rs875989805(T;T)
Alt rs875989805(T;T)
Reference rs875989805(C;C)
Significance Probable-Pathogenic
Disease Nance-Horan syndrome
Variation info
Gene NHS
CLNDBN Nance-Horan syndrome
Reversed 0
HGVS NC_000023.10:g.17705990C>T
CLNSRC
CLNACC RCV000211110.1,