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rs1057520790

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520790(A;A)
Make rs1057520790(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position53652988
GeneRPGRIP1L
is asnp
is mentioned by
dbSNPrs1057520790
dbSNP (old)rs1057520790
ClinGenrs1057520790
ebirs1057520790
HLIrs1057520790
Exacrs1057520790
Gnomadrs1057520790
Varsomers1057520790
Maprs1057520790
PheGenIrs1057520790
Biobankrs1057520790
1000 genomesrs1057520790
hgdprs1057520790
ensemblrs1057520790
gopubmedrs1057520790
geneviewrs1057520790
scholarrs1057520790
googlers1057520790
pharmgkbrs1057520790
gwascentralrs1057520790
openSNPrs1057520790
23andMers1057520790
23andMe allrs1057520790
SNPshotrs1057520790
SNPdbers1057520790
MSV3drs1057520790
GWAS Ctlgrs1057520790
Max Magnitude0
ClinVar
Risk rs1057520790(A;A)
Alt rs1057520790(A;A)
Reference Rs1057520790(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RPGRIP1L
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.53686900C>T
CLNSRC
CLNACC RCV000434303.1,