Have questions? Visit https://www.reddit.com/r/SNPedia

rs367576664

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs367576664(A;A)
Make rs367576664(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position75950867
GeneIMPG1
is asnp
is mentioned by
dbSNPrs367576664
ebirs367576664
HLIrs367576664
Exacrs367576664
Varsomers367576664
Maprs367576664
PheGenIrs367576664
hapmaprs367576664
1000 genomesrs367576664
hgdprs367576664
ensemblrs367576664
gopubmedrs367576664
geneviewrs367576664
scholarrs367576664
googlers367576664
pharmgkbrs367576664
gwascentralrs367576664
openSNPrs367576664
23andMers367576664
23andMe allrs367576664
SNP Nexus

SNPshotrs367576664
SNPdbers367576664
MSV3drs367576664
GWAS Ctlgrs367576664
Max Magnitude0
ClinVar
Risk rs367576664(A;A)
Alt rs367576664(A;A)
Reference rs367576664(G;G)
Significance Pathogenic
Disease Macular dystrophy
Variation info
Gene IMPG1
CLNDBN Macular dystrophy, vitelliform, 4
Reversed 0
HGVS NC_000006.11:g.76660584G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000149549.4,