Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.22 (C)
Location

Chromosome 10:101953705 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17880376, rs56743359

This variation has 4 HGVS names - click the plus to show

10:g.101953705A>C
ENST00000588656.1:n.96+36T>G
ENST00000590930.1:n.1995T>G
ENST00000370397.7:c.1974+36T>G

This variation has assays on 6 chips - click the plus to show

Variation displays