Variant (rsID / SNP)

rs34603556

rs34603556 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCB5. Location: chromosome 7, position 20,691,047. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ABCB5Not classified

Variant type: start_lost
Chromosome / position: 7:20691047
HGVS: NM_001163942.2,c.2T>C,p.Met1?
Allele change: Missense_M446T

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.