Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 11:69809573 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.69809573G>C

About this variant

This variant overlaps 1 transcript and has 1 individual genotype.

Variation displays