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rs672601326

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs672601326(-;-)
Make rs672601326(-;TACT)
Make rs672601326(TACT;TACT)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position42721913
GenePRPH2
is asnp
is mentioned by
dbSNPrs672601326
ebirs672601326
HLIrs672601326
Exacrs672601326
Varsomers672601326
Maprs672601326
PheGenIrs672601326
hapmaprs672601326
1000 genomesrs672601326
hgdprs672601326
ensemblrs672601326
gopubmedrs672601326
geneviewrs672601326
scholarrs672601326
googlers672601326
pharmgkbrs672601326
gwascentralrs672601326
openSNPrs672601326
23andMers672601326
23andMe allrs672601326
SNP Nexus

SNPshotrs672601326
SNPdbers672601326
MSV3drs672601326
GWAS Ctlgrs672601326
Max Magnitude0
ClinVar
Risk rs672601326(TACT;TACT)
Alt rs672601326(TACT;TACT)
Reference rs672601326(;)
Significance Pathogenic
Disease Patterned dystrophy of retinal pigment epithelium
Variation info
Gene PRPH2
CLNDBN Patterned dystrophy of retinal pigment epithelium
Reversed 1
HGVS NC_000006.11:g.42689652_42689655dupAGTA
CLNSRC OMIM Allelic Variant
CLNACC RCV000014060.24,