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rs1057518122

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518122(A;A)
Make rs1057518122(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position21334710
GeneRPGRIP1
is asnp
is mentioned by
dbSNPrs1057518122
dbSNP (old)rs1057518122
ClinGenrs1057518122
ebirs1057518122
HLIrs1057518122
Exacrs1057518122
Gnomadrs1057518122
Varsomers1057518122
Maprs1057518122
PheGenIrs1057518122
Biobankrs1057518122
1000 genomesrs1057518122
hgdprs1057518122
ensemblrs1057518122
gopubmedrs1057518122
geneviewrs1057518122
scholarrs1057518122
googlers1057518122
pharmgkbrs1057518122
gwascentralrs1057518122
openSNPrs1057518122
23andMers1057518122
23andMe allrs1057518122
SNPshotrs1057518122
SNPdbers1057518122
MSV3drs1057518122
GWAS Ctlgrs1057518122
Max Magnitude0
ClinVar
Risk rs1057518122(A;A)
Alt rs1057518122(A;A)
Reference Rs1057518122(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RPGRIP1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.21802869G>A
CLNSRC
CLNACC RCV000413987.1,