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rs766251466

From SNPedia

Orientationplus
Geno Mag Summary
(GAG;GAG) 0 common in clinvar
Make rs766251466(-;-)
Make rs766251466(-;GAG)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position3916956
GeneMIR103A2, PANK2
is asnp
is mentioned by
dbSNPrs766251466
ebirs766251466
HLIrs766251466
Exacrs766251466
Varsomers766251466
Maprs766251466
PheGenIrs766251466
hapmaprs766251466
1000 genomesrs766251466
hgdprs766251466
ensemblrs766251466
gopubmedrs766251466
geneviewrs766251466
scholarrs766251466
googlers766251466
pharmgkbrs766251466
gwascentralrs766251466
openSNPrs766251466
23andMers766251466
23andMe allrs766251466
SNP Nexus

SNPshotrs766251466
SNPdbers766251466
MSV3drs766251466
GWAS Ctlgrs766251466
Max Magnitude0
ClinVar
Risk rs766251466(;)
Alt rs766251466(;)
Reference rs766251466(GAG;GAG)
Significance Pathogenic
Disease Pigmentary pallidal degeneration
Variation info
Gene MIR103A2 PANK2
CLNDBN Pigmentary pallidal degeneration
Reversed 0
HGVS NC_000020.10:g.3897603_3897605delGAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000004822.2,