Original source

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

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

Chromosome 6:34427896 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

6:g.34427896C>T

About this variant

This variant overlaps 8 transcripts and has 1103 individual genotypes.

Variation displays