Original source

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

Alleles
-/TTCT
Location

Chromosome 22: between 37255238 and 37255239 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59721298, rs34231070

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

Variation displays