Original source

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

Alleles
GGGGGCC/-
Location

Chromosome 2:75114563-75114569 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs34415979

This variation has 3 HGVS names - click the plus to show

Variation displays