Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.06 (T)
Location

Chromosome 7:92779015 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57523974, rs17696703

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 2 transcripts, has 3904 sample genotypes and is mentioned in 3 citations.

Variant displays