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rs879253775

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs879253775(C;C)
Make rs879253775(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position75120534
GeneNEK9
is asnp
is mentioned by
dbSNPrs879253775
ebirs879253775
HLIrs879253775
Exacrs879253775
Varsomers879253775
Maprs879253775
PheGenIrs879253775
hapmaprs879253775
1000 genomesrs879253775
hgdprs879253775
ensemblrs879253775
gopubmedrs879253775
geneviewrs879253775
scholarrs879253775
googlers879253775
pharmgkbrs879253775
gwascentralrs879253775
openSNPrs879253775
23andMers879253775
23andMe allrs879253775
SNP Nexus

SNPshotrs879253775
SNPdbers879253775
MSV3drs879253775
GWAS Ctlgrs879253775
Max Magnitude0
ClinVar
Risk rs879253775(C;C)
Alt rs879253775(C;C)
Reference rs879253775(T;T)
Significance Pathogenic
Disease Nevus comedonicus
Variation info
Gene NEK9
CLNDBN Nevus comedonicus
Reversed 1
HGVS NC_000014.8:g.75587237A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000234968.1,