Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: 0.21 (C)
Location

Chromosome 4:155211295 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60721603

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 5 transcripts, has 2575 sample genotypes and is mentioned in 1 citation.

Variant displays