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rs770461067

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;A) 3 Carrier of an autosomal recessive polycystic kidney disease mutation
(A;A) 0 common/normal


Make rs770461067(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position51659489
GeneLOC105375087, PKHD1
is asnp
is mentioned by
dbSNPrs770461067
ClinGenrs770461067
ebirs770461067
HLIrs770461067
Exacrs770461067
Varsomers770461067
Maprs770461067
PheGenIrs770461067
hapmaprs770461067
1000 genomesrs770461067
hgdprs770461067
ensemblrs770461067
gopubmedrs770461067
geneviewrs770461067
scholarrs770461067
googlers770461067
pharmgkbrs770461067
gwascentralrs770461067
openSNPrs770461067
23andMers770461067
23andMe allrs770461067
SNP Nexus

SNPshotrs770461067
SNPdbers770461067
MSV3drs770461067
GWAS Ctlgrs770461067
Max Magnitude3
ClinVar
Risk rs770461067(-;-)
Alt rs770461067(-;-)
Reference Rs770461067(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PKHD1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.51524287delA
CLNSRC
CLNACC RCV000308290.1,