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rs1057518097

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518097(C;G)
Make rs1057518097(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position54629521
GeneRP1
is asnp
is mentioned by
dbSNPrs1057518097
dbSNP (old)rs1057518097
ClinGenrs1057518097
ebirs1057518097
HLIrs1057518097
Exacrs1057518097
Gnomadrs1057518097
Varsomers1057518097
Maprs1057518097
PheGenIrs1057518097
Biobankrs1057518097
1000 genomesrs1057518097
hgdprs1057518097
ensemblrs1057518097
gopubmedrs1057518097
geneviewrs1057518097
scholarrs1057518097
googlers1057518097
pharmgkbrs1057518097
gwascentralrs1057518097
openSNPrs1057518097
23andMers1057518097
23andMe allrs1057518097
SNPshotrs1057518097
SNPdbers1057518097
MSV3drs1057518097
GWAS Ctlgrs1057518097
Max Magnitude0
ClinVar
Risk rs1057518097(G;G)
Alt rs1057518097(G;G)
Reference Rs1057518097(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RP1
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.55542081C>G
CLNSRC
CLNACC RCV000414196.1,