Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
-/GCT
Location

Chromosome 11: between 120138353 and 120138354 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs147304777

This variation has 4 HGVS names - click the plus to show

Variation displays