Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

A/-/AA/AAAA | Ancestral: A

Chromosome 6:144062495 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs71881634, rs61024620

This variation has 33 HGVS names - click the plus to show

About this variant

This variant overlaps 30 transcripts and has 1 individual genotype.

Variation displays