Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Co-located variant

dbSNP rs4145259 (C/A/T)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs376062733

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2510 sample genotypes.

Variant displays