Original source

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

CTTTC/- | MAF: 0.33 (-)

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

Most severe consequence
Evidence status


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

About this variant

This variant overlaps 3 transcripts, has 1184 individual genotypes and is mentioned in 1 citation.

Variation displays