Original source

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

Alleles
C/- | Ancestral: C | MAF: 0.46 (-)
Location

Chromosome 10:98468404 (forward strand) | View in location tab

Co-located

with dbSNP rs4145259 (C/A/T)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs376062733

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2510 sample genotypes.

Variant displays