Original source

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

G/A/C | Ancestral: G | Ambiguity code: V

Chromosome 6:161973317 (forward strand) | View in location tab


with COSMIC COSM3722940 (G/A), COSM98176 (G/A) ; HGMD-PUBLIC CM983422, CM030926

Most severe consequence
Evidence status

Clinical significance


LSDB 11237, 11255

This variation has 30 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

About this variant

This variant overlaps 14 transcripts and is associated with 4 phenotypes.

Variation displays