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rs864309679

From SNPedia

Orientationplus
Make rs864309679(-;-)
Make rs864309679(-;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position17726876
GeneNHS
is asnp
is mentioned by
dbSNPrs864309679
ebirs864309679
HLIrs864309679
Exacrs864309679
Varsomers864309679
Maprs864309679
PheGenIrs864309679
hapmaprs864309679
1000 genomesrs864309679
hgdprs864309679
ensemblrs864309679
gopubmedrs864309679
geneviewrs864309679
scholarrs864309679
googlers864309679
pharmgkbrs864309679
gwascentralrs864309679
openSNPrs864309679
23andMers864309679
23andMe allrs864309679
SNP Nexus

SNPshotrs864309679
SNPdbers864309679
MSV3drs864309679
GWAS Ctlgrs864309679
Max Magnitude
ClinVar
Risk rs864309679(;)
Alt rs864309679(;)
Reference rs864309679(G;G)
Significance Pathogenic
Disease Congenital cataract
Variation info
Gene NHS
CLNDBN Congenital cataract
Reversed 0
HGVS NC_000023.10:g.17744996delG
CLNSRC
CLNACC RCV000203327.1,