Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: < 0.01 (C)
Location

Chromosome 1:12165876 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.12165876T>C

About this variant

This variant overlaps 4 transcripts, has 1170 individual genotypes and is mentioned in 1 citation.

Variation displays