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rs1057517879

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(GTT;GTT) 0 common in clinvar
Make rs1057517879(-;-)
Make rs1057517879(-;TTG)
Make rs1057517879(TTG;TTG)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position20218202
GeneATP6V1B2
is asnp
is mentioned by
dbSNPrs1057517879
dbSNP (old)rs1057517879
ClinGenrs1057517879
ebirs1057517879
HLIrs1057517879
Exacrs1057517879
Gnomadrs1057517879
Varsomers1057517879
Maprs1057517879
PheGenIrs1057517879
Biobankrs1057517879
1000 genomesrs1057517879
hgdprs1057517879
ensemblrs1057517879
gopubmedrs1057517879
geneviewrs1057517879
scholarrs1057517879
googlers1057517879
pharmgkbrs1057517879
gwascentralrs1057517879
openSNPrs1057517879
23andMers1057517879
23andMe allrs1057517879
SNPshotrs1057517879
SNPdbers1057517879
MSV3drs1057517879
GWAS Ctlgrs1057517879
Max Magnitude0
ClinVar
Risk rs1057517879(-;-)
Alt rs1057517879(-;-)
Reference Rs1057517879(GTT;GTT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATP6V1B2
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.20075713_20075715delTTG
CLNSRC
CLNACC RCV000414094.1,