Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.48 (C)
Location

Chromosome 20:63337540 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs61065182, rs17817947

HGVS name

20:g.63337540C>T

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 4035 sample genotypes and is mentioned in 1 citation.

Variant displays