Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.15 (T)
Location

Chromosome 1:153561551 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

This variant has 12 HGVS names - click the plus to show

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 4020 sample genotypes and is mentioned in 1 citation.

Variant displays