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rs1020621286

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position51772791
GenePKHD1
is asnp
is mentioned by
dbSNPrs1020621286
dbSNP (classic)rs1020621286
ClinGenrs1020621286
ebirs1020621286
HLIrs1020621286
Exacrs1020621286
Gnomadrs1020621286
Varsomers1020621286
LitVarrs1020621286
Maprs1020621286
PheGenIrs1020621286
Biobankrs1020621286
1000 genomesrs1020621286
hgdprs1020621286
ensemblrs1020621286
geneviewrs1020621286
scholarrs1020621286
googlers1020621286
pharmgkbrs1020621286
gwascentralrs1020621286
openSNPrs1020621286
23andMers1020621286
23andMe allrs1020621286
SNPshotrs1020621286
SNPdbers1020621286
MSV3drs1020621286
GWAS Ctlgrs1020621286
Max Magnitude0
ClinVar
Risk rs1020621286(G;G)
Alt rs1020621286(G;G)
Reference Rs1020621286(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PKHD1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.51637589T>G
CLNSRC
CLNACC RCV000492982.1,