Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y
Location

Chromosome 4:53431633 (forward strand)|View in location tab

Co-located variant

dbSNP rs58637505 (C/-)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs71621066

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 260 sample genotypes.

Variant displays