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rs1057519616

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057519616(-;C)
Make rs1057519616(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position56453607
GeneMIP
is asnp
is mentioned by
dbSNPrs1057519616
dbSNP (old)rs1057519616
ClinGenrs1057519616
ebirs1057519616
HLIrs1057519616
Exacrs1057519616
Gnomadrs1057519616
Varsomers1057519616
Maprs1057519616
PheGenIrs1057519616
Biobankrs1057519616
1000 genomesrs1057519616
hgdprs1057519616
ensemblrs1057519616
gopubmedrs1057519616
geneviewrs1057519616
scholarrs1057519616
googlers1057519616
pharmgkbrs1057519616
gwascentralrs1057519616
openSNPrs1057519616
23andMers1057519616
23andMe allrs1057519616
SNPshotrs1057519616
SNPdbers1057519616
MSV3drs1057519616
GWAS Ctlgrs1057519616
Max Magnitude0
ClinVar
Risk rs1057519616(C;C)
Alt rs1057519616(C;C)
Reference Rs1057519616(-;-)
Significance Pathogenic
Disease Cataract 15
Variation info
Gene MIP
CLNDBN Cataract 15, multiple types
Reversed 1
HGVS NC_000012.11:g.56847392dupG
CLNSRC
CLNACC RCV000420543.1,