Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.26 (T)
Location

Chromosome 7:75947638 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and has 2509 sample genotypes.

Variant displays