Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

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

Variant displays