Original source

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

Alleles
-/CGG
Location

Chromosome 4: between 146639340 and 146639341 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 1 individual genotype.

Variation displays