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rs786205623

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205623(-;-)
Make rs786205623(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position21327785
GeneRPGRIP1
is asnp
is mentioned by
dbSNPrs786205623
ebirs786205623
HLIrs786205623
Exacrs786205623
Varsomers786205623
Maprs786205623
PheGenIrs786205623
hapmaprs786205623
1000 genomesrs786205623
hgdprs786205623
ensemblrs786205623
gopubmedrs786205623
geneviewrs786205623
scholarrs786205623
googlers786205623
pharmgkbrs786205623
gwascentralrs786205623
openSNPrs786205623
23andMers786205623
23andMe allrs786205623
SNP Nexus

SNPshotrs786205623
SNPdbers786205623
MSV3drs786205623
GWAS Ctlgrs786205623
Max Magnitude0
ClinVar
Risk rs786205623(;)
Alt rs786205623(;)
Reference rs786205623(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RPGRIP1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.21795944delA
CLNSRC
CLNACC RCV000171475.1,