Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.01 (T)
Location

Chromosome 1:229282184 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs342863, rs368446, rs1194065

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2506 sample genotypes.

Variant displays