Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.06 (C)
Location

Chromosome 10:27744504 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57846316

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2510 sample genotypes.

Variant displays