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rs200846354

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200846354(A;A)
Make rs200846354(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position10608139
GeneRP1L1
is asnp
is mentioned by
dbSNPrs200846354
dbSNP (classic)rs200846354
ClinGenrs200846354
ebirs200846354
HLIrs200846354
Exacrs200846354
Gnomadrs200846354
Varsomers200846354
LitVarrs200846354
Maprs200846354
PheGenIrs200846354
Biobankrs200846354
1000 genomesrs200846354
hgdprs200846354
ensemblrs200846354
geneviewrs200846354
scholarrs200846354
googlers200846354
pharmgkbrs200846354
gwascentralrs200846354
openSNPrs200846354
23andMers200846354
23andMe allrs200846354
SNPshotrs200846354
SNPdbers200846354
MSV3drs200846354
GWAS Ctlgrs200846354
Max Magnitude0
ClinVar
Risk rs200846354(A;A)
Alt rs200846354(A;A)
Reference Rs200846354(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RP1L1
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.10465649G>A
CLNSRC
CLNACC RCV000487849.1,