Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.12 (C)
Location

Chromosome 1:167287553 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60788541

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, has 2894 sample genotypes and is mentioned in 1 citation.

Variant displays