Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.03 (T)
Location

Chromosome 2:208121161 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs17460066

HGVS name

2:g.208121161C>T

About this variant

This variant overlaps 1 transcript, has 2845 sample genotypes and is mentioned in 1 citation.

Variant displays