Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.02 (T)
Location

Chromosome 1:115287199 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60290047, rs3730213

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2804 sample genotypes.

Variant displays