Original source

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

Alleles
-/G/GTC/GTCT
Location

Chromosome 1: between 236815695 and 236815696 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs200394864, rs112130300

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 10 sample genotypes.

Variant displays