Variant (rsID / SNP)

rs1198849

rs1198849 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP6V1C2. Location: chromosome 2, position 10,908,893. The table records no clinical significance for this variant.

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Reference-table entries

ATP6V1C2Not classified

Variant type: missense_variant
Chromosome / position: 2:10908893
HGVS: NM_001039362.2,c.427A>G,p.Asn143Asp
Allele change: Missense_N143D

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.