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rs398124239

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124239(-;-)
Make rs398124239(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position46854004
GeneRP2
is asnp
is mentioned by
dbSNPrs398124239
ebirs398124239
HLIrs398124239
Exacrs398124239
Varsomers398124239
Maprs398124239
PheGenIrs398124239
hapmaprs398124239
1000 genomesrs398124239
hgdprs398124239
ensemblrs398124239
gopubmedrs398124239
geneviewrs398124239
scholarrs398124239
googlers398124239
pharmgkbrs398124239
gwascentralrs398124239
openSNPrs398124239
23andMers398124239
23andMe allrs398124239
SNP Nexus

SNPshotrs398124239
SNPdbers398124239
MSV3drs398124239
GWAS Ctlgrs398124239
Max Magnitude0
ClinVar
Risk rs398124239(;)
Alt rs398124239(;)
Reference rs398124239(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RP2
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.46713439delC
CLNSRC ClinVar
CLNACC RCV000081468.4,