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Variant (rsID / SNP)

rs6848883

ASIC5

rs6848883 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ASIC5. Location: chromosome 4, position 156,787,340. The table records no clinical significance for this variant.

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Reference-table entries

ASIC5Not classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
4:156787340
HGVS
NM_017419.3,c.39C>T,p.Asn13Asn
Allele change
Synonymous_N13N

Public references

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