Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/-/TT | Ancestral: T
Location

Chromosome 11:102599030 (forward strand) | View in location tab

Co-located

with dbSNP rs372588239 (T/G)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61110135, rs151047297

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

Variation displays