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rs369588002

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs369588002(A;A)
Make rs369588002(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position100990470
GeneC10orf2
is asnp
is mentioned by
dbSNPrs369588002
ebirs369588002
HLIrs369588002
Exacrs369588002
Varsomers369588002
Maprs369588002
PheGenIrs369588002
hapmaprs369588002
1000 genomesrs369588002
hgdprs369588002
ensemblrs369588002
gopubmedrs369588002
geneviewrs369588002
scholarrs369588002
googlers369588002
pharmgkbrs369588002
gwascentralrs369588002
openSNPrs369588002
23andMers369588002
23andMe allrs369588002
SNP Nexus

SNPshotrs369588002
SNPdbers369588002
MSV3drs369588002
GWAS Ctlgrs369588002
Max Magnitude0
ClinVar
Risk rs369588002(A;A)
Alt rs369588002(A;A)
Reference rs369588002(G;G)
Significance Pathogenic
Disease Perrault syndrome 5
Variation info
Gene C10orf2
CLNDBN Perrault syndrome 5
Reversed 0
HGVS NC_000010.10:g.102750227G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000149473.5,