Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.17 (A)
Location

Chromosome 1:7977436 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1173410, rs17367108, rs526595

This variation has 8 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 3865 individual genotypes and is mentioned in 2 citations.

Variation displays