Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.42 (T)
Location

Chromosome 9:101435495 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 2775 sample genotypes and is mentioned in 1 citation.

Variant displays