This variant has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A/C/T|Ancestral: G|Ambiguity code: N|MAF: < 0.01 (A)
Location

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

Co-located variants

COSMIC COSM3722940, COSM98176 ; HGMD-PUBLIC CM030926, CM983422

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 11237, 11255

HGVS names

This variant has 45 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 21 transcripts, has 2504 sample genotypes and is associated with 4 phenotypes.

Variant displays