Original source

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

Alleles
C/G|Ancestral: G|Ambiguity code: S
Location

Chromosome 5:41739892 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs661720

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 3 sample genotypes.

Variant displays