Original source

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

Alleles
-/T
Location

Chromosome 7: between 103498449 and 103498450 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs200006453, rs142568772

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

Variation displays