Original source

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

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

Chromosome 11:44564126 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.44564126C>T

About this variant

This variant overlaps 9 transcripts and has 1 individual genotype.

Variation displays