Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.03 (C)
Location

Chromosome 1:219916709 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59358060

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 2775 sample genotypes.

Variant displays