Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.16 (G)
Location

Chromosome 1:7963610 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs1173411

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2508 sample genotypes.

Variant displays