Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 1:10420271 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs3204495

HGVS name

1:g.10420271A>C

About this variant

This variant overlaps 5 transcripts and has 2 sample genotypes.

Variant displays