Variant (rsID / SNP)

rs121964881

rs121964881 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP6V1B1. Location: chromosome 2, position 71,185,233. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

ATP6V1B1Pathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 2:71185233
Cytoband: 2p13.3
HGVS: NM_001692.4(ATP6V1B1):c.232G>A (p.Gly78Arg)
Allele change: Missense_G78R

Associated conditions / phenotypes

Renal tubular acidosis with progressive nerve deafness|Inborn genetic diseases

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.