Original source

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

T/A/G | Ancestral: T | Ambiguity code: D

Chromosome 6:32578852 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs34274884, rs3816985

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and is mentioned in 1 citation.

Variation displays