Original source

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

Alleles
-/C/CC|MAF: 0.49 (-)
Location

Chromosome 15: between 42949600 and 42949601 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs140634913

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2511 sample genotypes.

Variant displays