Original source

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

C/T | Ancestral: C | Ambiguity code: Y

Chromosome 11:6392036 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


This variant has 3 synonyms - Show

HGVS names

This variant has 15 HGVS names - Show

About this variant

This variant overlaps 27 transcripts and has 262 sample genotypes.

Variant displays