Original source

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

Alleles
T/C|Ambiguity code: Y
Location

Chromosome 4:136443949 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 7 sample genotypes.

Variant displays