Original source

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

Alleles
-/T
Location

Chromosome 8: between 22916004 and 22916005 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs370466030, rs200849711

This variation has 6 HGVS names - click the plus to show

Variation displays