Original source

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

Alleles
T/G | Ambiguity code: K
Location

Chromosome 6:111606615 (forward strand) | View in location tab

Co-located

with dbSNP rs61374253 (-/TGGGGG/TG/GGGGT/GGGGGT/GT)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58747618

HGVS name

6:g.111606615T>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5

Variation displays