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rs786205626

From SNPedia

Orientationminus
Geno Mag Summary
(TTCCTGCGCTTC;TTCCTGCGCTTC) 0 common in clinvar
Make rs786205626(-;-)
Make rs786205626(-;TTCCTGCGCTTC)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89217169
GeneRLBP1
is asnp
is mentioned by
dbSNPrs786205626
ebirs786205626
HLIrs786205626
Exacrs786205626
Varsomers786205626
Maprs786205626
PheGenIrs786205626
hapmaprs786205626
1000 genomesrs786205626
hgdprs786205626
ensemblrs786205626
gopubmedrs786205626
geneviewrs786205626
scholarrs786205626
googlers786205626
pharmgkbrs786205626
gwascentralrs786205626
openSNPrs786205626
23andMers786205626
23andMe allrs786205626
SNP Nexus

SNPshotrs786205626
SNPdbers786205626
MSV3drs786205626
GWAS Ctlgrs786205626
Max Magnitude0
ClinVar
Risk rs786205626(;)
Alt rs786205626(;)
Reference rs786205626(TTCCTGCGCTTC;TTCCTGCGCTTC)
Significance Probable-Pathogenic
Disease not provided Bothnia retinal dystrophy
Variation info
Gene RLBP1
CLNDBN not provided Bothnia retinal dystrophy
Reversed 1
HGVS NC_000015.9:g.89760400_89760411delGAAGCGCAGGAA
CLNSRC
CLNACC RCV000171480.1, RCV000197318.1,