Original source

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

Alleles
G/C | Ambiguity code: S | MAF: 0.16 (G)
Location

Chromosome 17:65008950 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61461477

HGVS name

17:g.65008950G>C

About this variant

This variant overlaps 2 transcripts and has 2851 individual genotypes.

Variation displays