Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.18 (C)
Location

Chromosome 5:135032710 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61679533

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 2506 sample genotypes and is mentioned in 1 citation.

Variant displays