Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
CTTTC/- | MAF: 0.32 (-)
Location

Chromosome 8:118935562-118935566 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 2596 individual genotypes and is mentioned in 1 citation.

Variation displays