Original source

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

Alleles
-/TCTT/TTCT
Location

Chromosome 22: between 37255235 and 37255236 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs138700220

This variation has 8 HGVS names - click the plus to show

Variation displays