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rs768660614

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs768660614(-;-)
Make rs768660614(-;T)
Make rs768660614(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position101320304
GeneIMPG2
is asnp
is mentioned by
dbSNPrs768660614
ebirs768660614
HLIrs768660614
Exacrs768660614
Varsomers768660614
Maprs768660614
PheGenIrs768660614
hapmaprs768660614
1000 genomesrs768660614
hgdprs768660614
ensemblrs768660614
gopubmedrs768660614
geneviewrs768660614
scholarrs768660614
googlers768660614
pharmgkbrs768660614
gwascentralrs768660614
openSNPrs768660614
23andMers768660614
23andMe allrs768660614
SNP Nexus

SNPshotrs768660614
SNPdbers768660614
MSV3drs768660614
GWAS Ctlgrs768660614
Max Magnitude0
ClinVar
Risk rs768660614(T;T)
Alt rs768660614(T;T)
Reference rs768660614(;)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene IMPG2
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000003.11:g.101039149dupT
CLNSRC
CLNACC RCV000225378.1,