Original source

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

Alleles
T/TTTTTTT/TTTTTT/TTTTT/-
Location

Chromosome 1:247693036 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 40 HGVS names - click the plus to show

Variation displays