Original source

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

Alleles
T/- | Ancestral: T
Location

Chromosome 1:38044596 (forward strand) | View in location tab

Co-located

with dbSNP rs62676861 (T/G)

Most severe consequence

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts.

Variation displays