Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 1:75127358 (forward strand) | View in location tab

Most severe consequence
HGVS name

1:g.75127358C>G

About this variant

This variant overlaps 4 transcripts and has 270 individual genotypes.

Variation displays