Original source

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

Alleles
G/C|Ancestral: C|Ambiguity code: S|MAF: 0.01 (G)
Location

Chromosome 2:208249074 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57877504

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 11 transcripts and has 2679 sample genotypes.

Variant displays