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rs398124354

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124354(A;A)
Make rs398124354(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position21327687
GeneRPGRIP1
is asnp
is mentioned by
dbSNPrs398124354
ebirs398124354
HLIrs398124354
Exacrs398124354
Varsomers398124354
Maprs398124354
PheGenIrs398124354
hapmaprs398124354
1000 genomesrs398124354
hgdprs398124354
ensemblrs398124354
gopubmedrs398124354
geneviewrs398124354
scholarrs398124354
googlers398124354
pharmgkbrs398124354
gwascentralrs398124354
openSNPrs398124354
23andMers398124354
23andMe allrs398124354
SNP Nexus

SNPshotrs398124354
SNPdbers398124354
MSV3drs398124354
GWAS Ctlgrs398124354
Max Magnitude0
ClinVar
Risk rs398124354(A;A)
Alt rs398124354(A;A)
Reference rs398124354(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RPGRIP1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.21795846G>A
CLNSRC ClinVar
CLNACC RCV000082001.4,