Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 1:186671571 (forward strand) | View in location tab

Co-located

with dbSNP rs374840908 (G/GC/TT/T)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs79035632, rs17581169

HGVS name

1:g.186671571G>T

Genotyping chips

This variation has assays on: Illumina_1M-duo

Variation displays