Original source

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

Alleles
C/T|Ambiguity code: Y
Location

Chromosome 1:120488394 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs1778134, rs3843065

HGVS name

1:g.120488394C>T

About this variant

This variant overlaps 1 transcript and has 5 sample genotypes.

Variant displays