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rs864309696

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs864309696(-;GGGAACATTCCACT)
Make rs864309696(GGGAACATTCCACT;GGGAACATTCCACT)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position56453080
GeneMIP
is asnp
is mentioned by
dbSNPrs864309696
ClinGenrs864309696
ebirs864309696
HLIrs864309696
Exacrs864309696
Varsomers864309696
Maprs864309696
PheGenIrs864309696
hapmaprs864309696
1000 genomesrs864309696
hgdprs864309696
ensemblrs864309696
gopubmedrs864309696
geneviewrs864309696
scholarrs864309696
googlers864309696
pharmgkbrs864309696
gwascentralrs864309696
openSNPrs864309696
23andMers864309696
23andMe allrs864309696
SNP Nexus

SNPshotrs864309696
SNPdbers864309696
MSV3drs864309696
GWAS Ctlgrs864309696
Max Magnitude0
ClinVar
Risk rs864309696(GGGAACATTCCACT;GGGAACATTCCACT)
Alt rs864309696(GGGAACATTCCACT;GGGAACATTCCACT)
Reference Rs864309696(;)
Significance Pathogenic
Disease Congenital cataract
Variation info
Gene MIP
CLNDBN Congenital cataract
Reversed 1
HGVS NC_000012.11:g.56846864_56846865insAGTGGAATGTTCCC
CLNSRC
CLNACC RCV000203358.1,