Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


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