Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S|MAF: 0.48 (G)
Location

Chromosome 7:30965828 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61654257

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 6 transcripts, has 2772 sample genotypes and is mentioned in 1 citation.

Variant displays