Original source

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

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

Chromosome 1:161236056 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

This variant has 33 HGVS names - click the plus to show

About this variant

This variant overlaps 35 transcripts and has 356 sample genotypes.

Variant displays