Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs3765966

CA6

rs3765966 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CA6. Location: chromosome 1, position 9,011,722. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

CA6Not classified
Variant type
intron_variant
Chromosome / position
1:9011722
HGVS
NM_001270500.2,c.259+2221G>T
Allele change
Silent

Public references

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