Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.23 (C)
Location

Chromosome 20:37097648 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

20:g.37097648C>T

About this variant

This variant overlaps 8 transcripts and has 2581 sample genotypes.

Variant displays